Natural and artificial light-harvesting systems utilizing the functions of carotenoids
Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example...
Ausführliche Beschreibung
Autor*in: |
Hashimoto, Hideki [verfasserIn] |
---|
Format: |
E-Artikel |
---|---|
Sprache: |
Englisch |
Erschienen: |
2015transfer abstract |
---|
Schlagwörter: |
---|
Umfang: |
25 |
---|
Übergeordnetes Werk: |
Enthalten in: The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ - Jing, Yue ELSEVIER, 2017transfer abstract, Amsterdam [u.a.] |
---|---|
Übergeordnetes Werk: |
volume:25 ; year:2015 ; pages:46-70 ; extent:25 |
Links: |
---|
DOI / URN: |
10.1016/j.jphotochemrev.2015.07.004 |
---|
Katalog-ID: |
ELV034383484 |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | ELV034383484 | ||
003 | DE-627 | ||
005 | 20230625200751.0 | ||
007 | cr uuu---uuuuu | ||
008 | 180603s2015 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.jphotochemrev.2015.07.004 |2 doi | |
028 | 5 | 2 | |a GBVA2015003000018.pica |
035 | |a (DE-627)ELV034383484 | ||
035 | |a (ELSEVIER)S1389-5567(15)00032-5 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
082 | 0 | |a 570 |a 540 | |
082 | 0 | 4 | |a 570 |q DE-600 |
082 | 0 | 4 | |a 540 |q DE-600 |
082 | 0 | 4 | |a 530 |q VZ |
082 | 0 | 4 | |a 670 |q VZ |
084 | |a 51.60 |2 bkl | ||
084 | |a 58.45 |2 bkl | ||
100 | 1 | |a Hashimoto, Hideki |e verfasserin |4 aut | |
245 | 1 | 0 | |a Natural and artificial light-harvesting systems utilizing the functions of carotenoids |
264 | 1 | |c 2015transfer abstract | |
300 | |a 25 | ||
336 | |a nicht spezifiziert |b zzz |2 rdacontent | ||
337 | |a nicht spezifiziert |b z |2 rdamedia | ||
338 | |a nicht spezifiziert |b zu |2 rdacarrier | ||
520 | |a Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. | ||
520 | |a Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. | ||
650 | 7 | |a NADPH |2 Elsevier | |
650 | 7 | |a CARS |2 Elsevier | |
650 | 7 | |a Chl |2 Elsevier | |
650 | 7 | |a PSII |2 Elsevier | |
650 | 7 | |a AFM |2 Elsevier | |
650 | 7 | |a Rba. |2 Elsevier | |
650 | 7 | |a TPE |2 Elsevier | |
650 | 7 | |a SeaWiFS |2 Elsevier | |
650 | 7 | |a IC |2 Elsevier | |
650 | 7 | |a Rsp. |2 Elsevier | |
650 | 7 | |a FWM |2 Elsevier | |
650 | 7 | |a FSM |2 Elsevier | |
650 | 7 | |a C–P |2 Elsevier | |
650 | 7 | |a PSI |2 Elsevier | |
650 | 7 | |a SWM |2 Elsevier | |
650 | 7 | |a FMO |2 Elsevier | |
650 | 7 | |a ET |2 Elsevier | |
650 | 7 | |a Blc. |2 Elsevier | |
650 | 7 | |a RC |2 Elsevier | |
650 | 7 | |a FCP |2 Elsevier | |
650 | 7 | |a ICM |2 Elsevier | |
650 | 7 | |a Bphe |2 Elsevier | |
650 | 7 | |a EET |2 Elsevier | |
650 | 7 | |a C–P–Q |2 Elsevier | |
650 | 7 | |a Bchl |2 Elsevier | |
650 | 7 | |a ICT |2 Elsevier | |
650 | 7 | |a Rps. |2 Elsevier | |
650 | 7 | |a ATP |2 Elsevier | |
650 | 7 | |a TEM |2 Elsevier | |
650 | 7 | |a C–P–C60 |2 Elsevier | |
700 | 1 | |a Sugai, Yuko |4 oth | |
700 | 1 | |a Uragami, Chiasa |4 oth | |
700 | 1 | |a Gardiner, Alastair T. |4 oth | |
700 | 1 | |a Cogdell, Richard J. |4 oth | |
773 | 0 | 8 | |i Enthalten in |n Elsevier Science |a Jing, Yue ELSEVIER |t The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ |d 2017transfer abstract |g Amsterdam [u.a.] |w (DE-627)ELV02060582X |
773 | 1 | 8 | |g volume:25 |g year:2015 |g pages:46-70 |g extent:25 |
856 | 4 | 0 | |u https://doi.org/10.1016/j.jphotochemrev.2015.07.004 |3 Volltext |
912 | |a GBV_USEFLAG_U | ||
912 | |a GBV_ELV | ||
912 | |a SYSFLAG_U | ||
912 | |a GBV_ILN_30 | ||
912 | |a GBV_ILN_60 | ||
936 | b | k | |a 51.60 |j Keramische Werkstoffe |j Hartstoffe |x Werkstoffkunde |q VZ |
936 | b | k | |a 58.45 |j Gesteinshüttenkunde |q VZ |
951 | |a AR | ||
952 | |d 25 |j 2015 |h 46-70 |g 25 | ||
953 | |2 045F |a 570 |
author_variant |
h h hh |
---|---|
matchkey_str |
hashimotohidekisugaiyukouragamichiasagar:2015----:auaadriiilihhretnssestlznteu |
hierarchy_sort_str |
2015transfer abstract |
bklnumber |
51.60 58.45 |
publishDate |
2015 |
allfields |
10.1016/j.jphotochemrev.2015.07.004 doi GBVA2015003000018.pica (DE-627)ELV034383484 (ELSEVIER)S1389-5567(15)00032-5 DE-627 ger DE-627 rakwb eng 570 540 570 DE-600 540 DE-600 530 VZ 670 VZ 51.60 bkl 58.45 bkl Hashimoto, Hideki verfasserin aut Natural and artificial light-harvesting systems utilizing the functions of carotenoids 2015transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 Elsevier Sugai, Yuko oth Uragami, Chiasa oth Gardiner, Alastair T. oth Cogdell, Richard J. oth Enthalten in Elsevier Science Jing, Yue ELSEVIER The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ 2017transfer abstract Amsterdam [u.a.] (DE-627)ELV02060582X volume:25 year:2015 pages:46-70 extent:25 https://doi.org/10.1016/j.jphotochemrev.2015.07.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_30 GBV_ILN_60 51.60 Keramische Werkstoffe Hartstoffe Werkstoffkunde VZ 58.45 Gesteinshüttenkunde VZ AR 25 2015 46-70 25 045F 570 |
spelling |
10.1016/j.jphotochemrev.2015.07.004 doi GBVA2015003000018.pica (DE-627)ELV034383484 (ELSEVIER)S1389-5567(15)00032-5 DE-627 ger DE-627 rakwb eng 570 540 570 DE-600 540 DE-600 530 VZ 670 VZ 51.60 bkl 58.45 bkl Hashimoto, Hideki verfasserin aut Natural and artificial light-harvesting systems utilizing the functions of carotenoids 2015transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 Elsevier Sugai, Yuko oth Uragami, Chiasa oth Gardiner, Alastair T. oth Cogdell, Richard J. oth Enthalten in Elsevier Science Jing, Yue ELSEVIER The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ 2017transfer abstract Amsterdam [u.a.] (DE-627)ELV02060582X volume:25 year:2015 pages:46-70 extent:25 https://doi.org/10.1016/j.jphotochemrev.2015.07.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_30 GBV_ILN_60 51.60 Keramische Werkstoffe Hartstoffe Werkstoffkunde VZ 58.45 Gesteinshüttenkunde VZ AR 25 2015 46-70 25 045F 570 |
allfields_unstemmed |
10.1016/j.jphotochemrev.2015.07.004 doi GBVA2015003000018.pica (DE-627)ELV034383484 (ELSEVIER)S1389-5567(15)00032-5 DE-627 ger DE-627 rakwb eng 570 540 570 DE-600 540 DE-600 530 VZ 670 VZ 51.60 bkl 58.45 bkl Hashimoto, Hideki verfasserin aut Natural and artificial light-harvesting systems utilizing the functions of carotenoids 2015transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 Elsevier Sugai, Yuko oth Uragami, Chiasa oth Gardiner, Alastair T. oth Cogdell, Richard J. oth Enthalten in Elsevier Science Jing, Yue ELSEVIER The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ 2017transfer abstract Amsterdam [u.a.] (DE-627)ELV02060582X volume:25 year:2015 pages:46-70 extent:25 https://doi.org/10.1016/j.jphotochemrev.2015.07.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_30 GBV_ILN_60 51.60 Keramische Werkstoffe Hartstoffe Werkstoffkunde VZ 58.45 Gesteinshüttenkunde VZ AR 25 2015 46-70 25 045F 570 |
allfieldsGer |
10.1016/j.jphotochemrev.2015.07.004 doi GBVA2015003000018.pica (DE-627)ELV034383484 (ELSEVIER)S1389-5567(15)00032-5 DE-627 ger DE-627 rakwb eng 570 540 570 DE-600 540 DE-600 530 VZ 670 VZ 51.60 bkl 58.45 bkl Hashimoto, Hideki verfasserin aut Natural and artificial light-harvesting systems utilizing the functions of carotenoids 2015transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 Elsevier Sugai, Yuko oth Uragami, Chiasa oth Gardiner, Alastair T. oth Cogdell, Richard J. oth Enthalten in Elsevier Science Jing, Yue ELSEVIER The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ 2017transfer abstract Amsterdam [u.a.] (DE-627)ELV02060582X volume:25 year:2015 pages:46-70 extent:25 https://doi.org/10.1016/j.jphotochemrev.2015.07.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_30 GBV_ILN_60 51.60 Keramische Werkstoffe Hartstoffe Werkstoffkunde VZ 58.45 Gesteinshüttenkunde VZ AR 25 2015 46-70 25 045F 570 |
allfieldsSound |
10.1016/j.jphotochemrev.2015.07.004 doi GBVA2015003000018.pica (DE-627)ELV034383484 (ELSEVIER)S1389-5567(15)00032-5 DE-627 ger DE-627 rakwb eng 570 540 570 DE-600 540 DE-600 530 VZ 670 VZ 51.60 bkl 58.45 bkl Hashimoto, Hideki verfasserin aut Natural and artificial light-harvesting systems utilizing the functions of carotenoids 2015transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 Elsevier Sugai, Yuko oth Uragami, Chiasa oth Gardiner, Alastair T. oth Cogdell, Richard J. oth Enthalten in Elsevier Science Jing, Yue ELSEVIER The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ 2017transfer abstract Amsterdam [u.a.] (DE-627)ELV02060582X volume:25 year:2015 pages:46-70 extent:25 https://doi.org/10.1016/j.jphotochemrev.2015.07.004 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_30 GBV_ILN_60 51.60 Keramische Werkstoffe Hartstoffe Werkstoffkunde VZ 58.45 Gesteinshüttenkunde VZ AR 25 2015 46-70 25 045F 570 |
language |
English |
source |
Enthalten in The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ Amsterdam [u.a.] volume:25 year:2015 pages:46-70 extent:25 |
sourceStr |
Enthalten in The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ Amsterdam [u.a.] volume:25 year:2015 pages:46-70 extent:25 |
format_phy_str_mv |
Article |
bklname |
Keramische Werkstoffe Hartstoffe Gesteinshüttenkunde |
institution |
findex.gbv.de |
topic_facet |
NADPH CARS Chl PSII AFM Rba. TPE SeaWiFS IC Rsp. FWM FSM C–P PSI SWM FMO ET Blc. RC FCP ICM Bphe EET C–P–Q Bchl ICT Rps. ATP TEM C–P–C60 |
dewey-raw |
570 |
isfreeaccess_bool |
false |
container_title |
The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ |
authorswithroles_txt_mv |
Hashimoto, Hideki @@aut@@ Sugai, Yuko @@oth@@ Uragami, Chiasa @@oth@@ Gardiner, Alastair T. @@oth@@ Cogdell, Richard J. @@oth@@ |
publishDateDaySort_date |
2015-01-01T00:00:00Z |
hierarchy_top_id |
ELV02060582X |
dewey-sort |
3570 |
id |
ELV034383484 |
language_de |
englisch |
fullrecord |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV034383484</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625200751.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2015 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.jphotochemrev.2015.07.004</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2015003000018.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV034383484</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S1389-5567(15)00032-5</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">570</subfield><subfield code="a">540</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">570</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">530</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">670</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">51.60</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">58.45</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Hashimoto, Hideki</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Natural and artificial light-harvesting systems utilizing the functions of carotenoids</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2015transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">25</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">NADPH</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">CARS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Chl</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PSII</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">AFM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Rba.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">TPE</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SeaWiFS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">IC</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Rsp.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FWM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FSM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">C–P</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PSI</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SWM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FMO</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ET</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Blc.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">RC</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FCP</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ICM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Bphe</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">EET</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">C–P–Q</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Bchl</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ICT</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Rps.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ATP</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">TEM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">C–P–C60</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Sugai, Yuko</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Uragami, Chiasa</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gardiner, Alastair T.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Cogdell, Richard J.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="a">Jing, Yue ELSEVIER</subfield><subfield code="t">The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+</subfield><subfield code="d">2017transfer abstract</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV02060582X</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:25</subfield><subfield code="g">year:2015</subfield><subfield code="g">pages:46-70</subfield><subfield code="g">extent:25</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.jphotochemrev.2015.07.004</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_30</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">51.60</subfield><subfield code="j">Keramische Werkstoffe</subfield><subfield code="j">Hartstoffe</subfield><subfield code="x">Werkstoffkunde</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">58.45</subfield><subfield code="j">Gesteinshüttenkunde</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">25</subfield><subfield code="j">2015</subfield><subfield code="h">46-70</subfield><subfield code="g">25</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">570</subfield></datafield></record></collection>
|
author |
Hashimoto, Hideki |
spellingShingle |
Hashimoto, Hideki ddc 570 ddc 540 ddc 530 ddc 670 bkl 51.60 bkl 58.45 Elsevier NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 Natural and artificial light-harvesting systems utilizing the functions of carotenoids |
authorStr |
Hashimoto, Hideki |
ppnlink_with_tag_str_mv |
@@773@@(DE-627)ELV02060582X |
format |
electronic Article |
dewey-ones |
570 - Life sciences; biology 540 - Chemistry & allied sciences 530 - Physics 670 - Manufacturing |
delete_txt_mv |
keep |
author_role |
aut |
collection |
elsevier |
remote_str |
true |
illustrated |
Not Illustrated |
topic_title |
570 540 570 DE-600 540 DE-600 530 VZ 670 VZ 51.60 bkl 58.45 bkl Natural and artificial light-harvesting systems utilizing the functions of carotenoids NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 Elsevier |
topic |
ddc 570 ddc 540 ddc 530 ddc 670 bkl 51.60 bkl 58.45 Elsevier NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 |
topic_unstemmed |
ddc 570 ddc 540 ddc 530 ddc 670 bkl 51.60 bkl 58.45 Elsevier NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 |
topic_browse |
ddc 570 ddc 540 ddc 530 ddc 670 bkl 51.60 bkl 58.45 Elsevier NADPH Elsevier CARS Elsevier Chl Elsevier PSII Elsevier AFM Elsevier Rba. Elsevier TPE Elsevier SeaWiFS Elsevier IC Elsevier Rsp. Elsevier FWM Elsevier FSM Elsevier C–P Elsevier PSI Elsevier SWM Elsevier FMO Elsevier ET Elsevier Blc. Elsevier RC Elsevier FCP Elsevier ICM Elsevier Bphe Elsevier EET Elsevier C–P–Q Elsevier Bchl Elsevier ICT Elsevier Rps. Elsevier ATP Elsevier TEM Elsevier C–P–C60 |
format_facet |
Elektronische Aufsätze Aufsätze Elektronische Ressource |
format_main_str_mv |
Text Zeitschrift/Artikel |
carriertype_str_mv |
zu |
author2_variant |
y s ys c u cu a t g at atg r j c rj rjc |
hierarchy_parent_title |
The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ |
hierarchy_parent_id |
ELV02060582X |
dewey-tens |
570 - Life sciences; biology 540 - Chemistry 530 - Physics 670 - Manufacturing |
hierarchy_top_title |
The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ |
isfreeaccess_txt |
false |
familylinks_str_mv |
(DE-627)ELV02060582X |
title |
Natural and artificial light-harvesting systems utilizing the functions of carotenoids |
ctrlnum |
(DE-627)ELV034383484 (ELSEVIER)S1389-5567(15)00032-5 |
title_full |
Natural and artificial light-harvesting systems utilizing the functions of carotenoids |
author_sort |
Hashimoto, Hideki |
journal |
The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ |
journalStr |
The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+ |
lang_code |
eng |
isOA_bool |
false |
dewey-hundreds |
500 - Science 600 - Technology |
recordtype |
marc |
publishDateSort |
2015 |
contenttype_str_mv |
zzz |
container_start_page |
46 |
author_browse |
Hashimoto, Hideki |
container_volume |
25 |
physical |
25 |
class |
570 540 570 DE-600 540 DE-600 530 VZ 670 VZ 51.60 bkl 58.45 bkl |
format_se |
Elektronische Aufsätze |
author-letter |
Hashimoto, Hideki |
doi_str_mv |
10.1016/j.jphotochemrev.2015.07.004 |
dewey-full |
570 540 530 670 |
title_sort |
natural and artificial light-harvesting systems utilizing the functions of carotenoids |
title_auth |
Natural and artificial light-harvesting systems utilizing the functions of carotenoids |
abstract |
Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. |
abstractGer |
Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. |
abstract_unstemmed |
Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced. |
collection_details |
GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_30 GBV_ILN_60 |
title_short |
Natural and artificial light-harvesting systems utilizing the functions of carotenoids |
url |
https://doi.org/10.1016/j.jphotochemrev.2015.07.004 |
remote_bool |
true |
author2 |
Sugai, Yuko Uragami, Chiasa Gardiner, Alastair T. Cogdell, Richard J. |
author2Str |
Sugai, Yuko Uragami, Chiasa Gardiner, Alastair T. Cogdell, Richard J. |
ppnlink |
ELV02060582X |
mediatype_str_mv |
z |
isOA_txt |
false |
hochschulschrift_bool |
false |
author2_role |
oth oth oth oth |
doi_str |
10.1016/j.jphotochemrev.2015.07.004 |
up_date |
2024-07-06T20:59:09.362Z |
_version_ |
1803864820272857088 |
fullrecord_marcxml |
<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>01000caa a22002652 4500</leader><controlfield tag="001">ELV034383484</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230625200751.0</controlfield><controlfield tag="007">cr uuu---uuuuu</controlfield><controlfield tag="008">180603s2015 xx |||||o 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1016/j.jphotochemrev.2015.07.004</subfield><subfield code="2">doi</subfield></datafield><datafield tag="028" ind1="5" ind2="2"><subfield code="a">GBVA2015003000018.pica</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)ELV034383484</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(ELSEVIER)S1389-5567(15)00032-5</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-627</subfield><subfield code="b">ger</subfield><subfield code="c">DE-627</subfield><subfield code="e">rakwb</subfield></datafield><datafield tag="041" ind1=" " ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">570</subfield><subfield code="a">540</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">570</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">540</subfield><subfield code="q">DE-600</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">530</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">670</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">51.60</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">58.45</subfield><subfield code="2">bkl</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Hashimoto, Hideki</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Natural and artificial light-harvesting systems utilizing the functions of carotenoids</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2015transfer abstract</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">25</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zzz</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">z</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">nicht spezifiziert</subfield><subfield code="b">zu</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Carotenoids are essential pigments in natural photosynthesis. They absorb in the blue–green region of the solar spectrum and transfer the absorbed energy to (bacterio-)chlorophylls, and so expand the wavelength range of light that is able to drive photosynthesis. This process is an example of singlet–singlet energy transfer and so carotenoids serve to enhance the overall efficiency of photosynthetic light reactions. Carotenoids also act to protect photosynthetic organisms from the harmful effects of excess exposure to light. In this case, triplet–triplet energy transfer from (bacterio-)chlorophyll to carotenoid plays a key role in this photoprotective reaction. In the light-harvesting pigment–protein complexes from purple photosynthetic bacteria and chlorophytes, carotenoids have an additional role, namely the structural stabilization of those complexes. In this article we review what is currently known about how carotenoids discharge these functions. The molecular architecture of photosynthetic systems will be outlined to provide a basis from which to describe the photochemistry of carotenoids, which underlies most of their important functions in photosynthesis. Then, the possibility to utilize the functions of carotenoids in artificial photosynthetic light-harvesting systems will be discussed. Some examples of the model systems are introduced.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">NADPH</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">CARS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Chl</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PSII</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">AFM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Rba.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">TPE</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SeaWiFS</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">IC</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Rsp.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FWM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FSM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">C–P</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">PSI</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">SWM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FMO</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ET</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Blc.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">RC</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">FCP</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ICM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Bphe</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">EET</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">C–P–Q</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Bchl</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ICT</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Rps.</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">ATP</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">TEM</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">C–P–C60</subfield><subfield code="2">Elsevier</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Sugai, Yuko</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Uragami, Chiasa</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gardiner, Alastair T.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Cogdell, Richard J.</subfield><subfield code="4">oth</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="n">Elsevier Science</subfield><subfield code="a">Jing, Yue ELSEVIER</subfield><subfield code="t">The first principles calculation and temperature-sensitive luminescence behavior of optimized red phosphor Mg2Al4Si5O18: Eu3+</subfield><subfield code="d">2017transfer abstract</subfield><subfield code="g">Amsterdam [u.a.]</subfield><subfield code="w">(DE-627)ELV02060582X</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:25</subfield><subfield code="g">year:2015</subfield><subfield code="g">pages:46-70</subfield><subfield code="g">extent:25</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="u">https://doi.org/10.1016/j.jphotochemrev.2015.07.004</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ELV</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_U</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_30</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_60</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">51.60</subfield><subfield code="j">Keramische Werkstoffe</subfield><subfield code="j">Hartstoffe</subfield><subfield code="x">Werkstoffkunde</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="936" ind1="b" ind2="k"><subfield code="a">58.45</subfield><subfield code="j">Gesteinshüttenkunde</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">25</subfield><subfield code="j">2015</subfield><subfield code="h">46-70</subfield><subfield code="g">25</subfield></datafield><datafield tag="953" ind1=" " ind2=" "><subfield code="2">045F</subfield><subfield code="a">570</subfield></datafield></record></collection>
|
score |
7.3986073 |