Palladium-catalyzed cycloaromatization polymerization of enediynes
Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymeri...
Ausführliche Beschreibung
Gespeichert in:
| Autor*in: |
Wang, Chonggang [verfasserIn] |
|---|
| Format: |
Artikel |
|---|---|
| Sprache: |
Englisch |
| Erschienen: |
2017 |
|---|
| Schlagwörter: |
|---|
| Anmerkung: |
© Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
|---|
| Übergeordnetes Werk: |
Enthalten in: Chinese journal of polymer science - Chinese Chemical Society and Institute of Chemistry, CAS, 1985, 36(2017), 2 vom: 01. Dez., Seite 237-243 |
|---|---|
| Übergeordnetes Werk: |
volume:36 ; year:2017 ; number:2 ; day:01 ; month:12 ; pages:237-243 |
| Links: |
|---|
| DOI / URN: |
10.1007/s10118-018-2088-9 |
|---|
| Katalog-ID: |
OLC2038273499 |
|---|
| LEADER | 01000caa a22002652 4500 | ||
|---|---|---|---|
| 001 | OLC2038273499 | ||
| 003 | DE-627 | ||
| 005 | 20230502172819.0 | ||
| 007 | tu | ||
| 008 | 200820s2017 xx ||||| 00| ||eng c | ||
| 024 | 7 | |a 10.1007/s10118-018-2088-9 |2 doi | |
| 035 | |a (DE-627)OLC2038273499 | ||
| 035 | |a (DE-He213)s10118-018-2088-9-p | ||
| 040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
| 041 | |a eng | ||
| 082 | 0 | 4 | |a 540 |a 660 |q VZ |
| 082 | 0 | 4 | |a 660 |a 670 |q VZ |
| 100 | 1 | |a Wang, Chonggang |e verfasserin |4 aut | |
| 245 | 1 | 0 | |a Palladium-catalyzed cycloaromatization polymerization of enediynes |
| 264 | 1 | |c 2017 | |
| 336 | |a Text |b txt |2 rdacontent | ||
| 337 | |a ohne Hilfsmittel zu benutzen |b n |2 rdamedia | ||
| 338 | |a Band |b nc |2 rdacarrier | ||
| 500 | |a © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 | ||
| 520 | |a Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. | ||
| 650 | 4 | |a Transition metal catalysis | |
| 650 | 4 | |a Enediyne | |
| 650 | 4 | |a Polymerization | |
| 650 | 4 | |a Cycloaromatization | |
| 650 | 4 | |a Bergman cyclization | |
| 700 | 1 | |a Chen, Shudan |4 aut | |
| 700 | 1 | |a Zhou, Hao |4 aut | |
| 700 | 1 | |a Gu, Jinlou |4 aut | |
| 700 | 1 | |a Hu, Aiguo |4 aut | |
| 773 | 0 | 8 | |i Enthalten in |t Chinese journal of polymer science |d Chinese Chemical Society and Institute of Chemistry, CAS, 1985 |g 36(2017), 2 vom: 01. Dez., Seite 237-243 |w (DE-627)130996939 |w (DE-600)1082856-4 |w (DE-576)026374684 |x 0256-7679 |7 nnns |
| 773 | 1 | 8 | |g volume:36 |g year:2017 |g number:2 |g day:01 |g month:12 |g pages:237-243 |
| 856 | 4 | 1 | |u https://doi.org/10.1007/s10118-018-2088-9 |z lizenzpflichtig |3 Volltext |
| 912 | |a GBV_USEFLAG_A | ||
| 912 | |a SYSFLAG_A | ||
| 912 | |a GBV_OLC | ||
| 912 | |a SSG-OLC-TEC | ||
| 912 | |a SSG-OLC-CHE | ||
| 912 | |a GBV_ILN_70 | ||
| 912 | |a GBV_ILN_267 | ||
| 912 | |a GBV_ILN_2018 | ||
| 912 | |a GBV_ILN_4277 | ||
| 951 | |a AR | ||
| 952 | |d 36 |j 2017 |e 2 |b 01 |c 12 |h 237-243 | ||
| author_variant |
c w cw s c sc h z hz j g jg a h ah |
|---|---|
| matchkey_str |
article:02567679:2017----::alductlzdylaoaiainoyei |
| hierarchy_sort_str |
2017 |
| publishDate |
2017 |
| allfields |
10.1007/s10118-018-2088-9 doi (DE-627)OLC2038273499 (DE-He213)s10118-018-2088-9-p DE-627 ger DE-627 rakwb eng 540 660 VZ 660 670 VZ Wang, Chonggang verfasserin aut Palladium-catalyzed cycloaromatization polymerization of enediynes 2017 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. Transition metal catalysis Enediyne Polymerization Cycloaromatization Bergman cyclization Chen, Shudan aut Zhou, Hao aut Gu, Jinlou aut Hu, Aiguo aut Enthalten in Chinese journal of polymer science Chinese Chemical Society and Institute of Chemistry, CAS, 1985 36(2017), 2 vom: 01. Dez., Seite 237-243 (DE-627)130996939 (DE-600)1082856-4 (DE-576)026374684 0256-7679 nnns volume:36 year:2017 number:2 day:01 month:12 pages:237-243 https://doi.org/10.1007/s10118-018-2088-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_267 GBV_ILN_2018 GBV_ILN_4277 AR 36 2017 2 01 12 237-243 |
| spelling |
10.1007/s10118-018-2088-9 doi (DE-627)OLC2038273499 (DE-He213)s10118-018-2088-9-p DE-627 ger DE-627 rakwb eng 540 660 VZ 660 670 VZ Wang, Chonggang verfasserin aut Palladium-catalyzed cycloaromatization polymerization of enediynes 2017 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. Transition metal catalysis Enediyne Polymerization Cycloaromatization Bergman cyclization Chen, Shudan aut Zhou, Hao aut Gu, Jinlou aut Hu, Aiguo aut Enthalten in Chinese journal of polymer science Chinese Chemical Society and Institute of Chemistry, CAS, 1985 36(2017), 2 vom: 01. Dez., Seite 237-243 (DE-627)130996939 (DE-600)1082856-4 (DE-576)026374684 0256-7679 nnns volume:36 year:2017 number:2 day:01 month:12 pages:237-243 https://doi.org/10.1007/s10118-018-2088-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_267 GBV_ILN_2018 GBV_ILN_4277 AR 36 2017 2 01 12 237-243 |
| allfields_unstemmed |
10.1007/s10118-018-2088-9 doi (DE-627)OLC2038273499 (DE-He213)s10118-018-2088-9-p DE-627 ger DE-627 rakwb eng 540 660 VZ 660 670 VZ Wang, Chonggang verfasserin aut Palladium-catalyzed cycloaromatization polymerization of enediynes 2017 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. Transition metal catalysis Enediyne Polymerization Cycloaromatization Bergman cyclization Chen, Shudan aut Zhou, Hao aut Gu, Jinlou aut Hu, Aiguo aut Enthalten in Chinese journal of polymer science Chinese Chemical Society and Institute of Chemistry, CAS, 1985 36(2017), 2 vom: 01. Dez., Seite 237-243 (DE-627)130996939 (DE-600)1082856-4 (DE-576)026374684 0256-7679 nnns volume:36 year:2017 number:2 day:01 month:12 pages:237-243 https://doi.org/10.1007/s10118-018-2088-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_267 GBV_ILN_2018 GBV_ILN_4277 AR 36 2017 2 01 12 237-243 |
| allfieldsGer |
10.1007/s10118-018-2088-9 doi (DE-627)OLC2038273499 (DE-He213)s10118-018-2088-9-p DE-627 ger DE-627 rakwb eng 540 660 VZ 660 670 VZ Wang, Chonggang verfasserin aut Palladium-catalyzed cycloaromatization polymerization of enediynes 2017 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. Transition metal catalysis Enediyne Polymerization Cycloaromatization Bergman cyclization Chen, Shudan aut Zhou, Hao aut Gu, Jinlou aut Hu, Aiguo aut Enthalten in Chinese journal of polymer science Chinese Chemical Society and Institute of Chemistry, CAS, 1985 36(2017), 2 vom: 01. Dez., Seite 237-243 (DE-627)130996939 (DE-600)1082856-4 (DE-576)026374684 0256-7679 nnns volume:36 year:2017 number:2 day:01 month:12 pages:237-243 https://doi.org/10.1007/s10118-018-2088-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_267 GBV_ILN_2018 GBV_ILN_4277 AR 36 2017 2 01 12 237-243 |
| allfieldsSound |
10.1007/s10118-018-2088-9 doi (DE-627)OLC2038273499 (DE-He213)s10118-018-2088-9-p DE-627 ger DE-627 rakwb eng 540 660 VZ 660 670 VZ Wang, Chonggang verfasserin aut Palladium-catalyzed cycloaromatization polymerization of enediynes 2017 Text txt rdacontent ohne Hilfsmittel zu benutzen n rdamedia Band nc rdacarrier © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. Transition metal catalysis Enediyne Polymerization Cycloaromatization Bergman cyclization Chen, Shudan aut Zhou, Hao aut Gu, Jinlou aut Hu, Aiguo aut Enthalten in Chinese journal of polymer science Chinese Chemical Society and Institute of Chemistry, CAS, 1985 36(2017), 2 vom: 01. Dez., Seite 237-243 (DE-627)130996939 (DE-600)1082856-4 (DE-576)026374684 0256-7679 nnns volume:36 year:2017 number:2 day:01 month:12 pages:237-243 https://doi.org/10.1007/s10118-018-2088-9 lizenzpflichtig Volltext GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_267 GBV_ILN_2018 GBV_ILN_4277 AR 36 2017 2 01 12 237-243 |
| language |
English |
| source |
Enthalten in Chinese journal of polymer science 36(2017), 2 vom: 01. Dez., Seite 237-243 volume:36 year:2017 number:2 day:01 month:12 pages:237-243 |
| sourceStr |
Enthalten in Chinese journal of polymer science 36(2017), 2 vom: 01. Dez., Seite 237-243 volume:36 year:2017 number:2 day:01 month:12 pages:237-243 |
| format_phy_str_mv |
Article |
| institution |
findex.gbv.de |
| topic_facet |
Transition metal catalysis Enediyne Polymerization Cycloaromatization Bergman cyclization |
| dewey-raw |
540 |
| isfreeaccess_bool |
false |
| container_title |
Chinese journal of polymer science |
| authorswithroles_txt_mv |
Wang, Chonggang @@aut@@ Chen, Shudan @@aut@@ Zhou, Hao @@aut@@ Gu, Jinlou @@aut@@ Hu, Aiguo @@aut@@ |
| publishDateDaySort_date |
2017-12-01T00:00:00Z |
| hierarchy_top_id |
130996939 |
| dewey-sort |
3540 |
| id |
OLC2038273499 |
| 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">OLC2038273499</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230502172819.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200820s2017 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10118-018-2088-9</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2038273499</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)s10118-018-2088-9-p</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="4"><subfield code="a">540</subfield><subfield code="a">660</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">660</subfield><subfield code="a">670</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Wang, Chonggang</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Palladium-catalyzed cycloaromatization polymerization of enediynes</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2017</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Transition metal catalysis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Enediyne</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Polymerization</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Cycloaromatization</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Bergman cyclization</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Chen, Shudan</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhou, Hao</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gu, Jinlou</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hu, Aiguo</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Chinese journal of polymer science</subfield><subfield code="d">Chinese Chemical Society and Institute of Chemistry, CAS, 1985</subfield><subfield code="g">36(2017), 2 vom: 01. Dez., Seite 237-243</subfield><subfield code="w">(DE-627)130996939</subfield><subfield code="w">(DE-600)1082856-4</subfield><subfield code="w">(DE-576)026374684</subfield><subfield code="x">0256-7679</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:36</subfield><subfield code="g">year:2017</subfield><subfield code="g">number:2</subfield><subfield code="g">day:01</subfield><subfield code="g">month:12</subfield><subfield code="g">pages:237-243</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/s10118-018-2088-9</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_267</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2018</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4277</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">36</subfield><subfield code="j">2017</subfield><subfield code="e">2</subfield><subfield code="b">01</subfield><subfield code="c">12</subfield><subfield code="h">237-243</subfield></datafield></record></collection>
|
| author |
Wang, Chonggang |
| spellingShingle |
Wang, Chonggang ddc 540 ddc 660 misc Transition metal catalysis misc Enediyne misc Polymerization misc Cycloaromatization misc Bergman cyclization Palladium-catalyzed cycloaromatization polymerization of enediynes |
| authorStr |
Wang, Chonggang |
| ppnlink_with_tag_str_mv |
@@773@@(DE-627)130996939 |
| format |
Article |
| dewey-ones |
540 - Chemistry & allied sciences 660 - Chemical engineering 670 - Manufacturing |
| delete_txt_mv |
keep |
| author_role |
aut aut aut aut aut |
| collection |
OLC |
| remote_str |
false |
| illustrated |
Not Illustrated |
| issn |
0256-7679 |
| topic_title |
540 660 VZ 660 670 VZ Palladium-catalyzed cycloaromatization polymerization of enediynes Transition metal catalysis Enediyne Polymerization Cycloaromatization Bergman cyclization |
| topic |
ddc 540 ddc 660 misc Transition metal catalysis misc Enediyne misc Polymerization misc Cycloaromatization misc Bergman cyclization |
| topic_unstemmed |
ddc 540 ddc 660 misc Transition metal catalysis misc Enediyne misc Polymerization misc Cycloaromatization misc Bergman cyclization |
| topic_browse |
ddc 540 ddc 660 misc Transition metal catalysis misc Enediyne misc Polymerization misc Cycloaromatization misc Bergman cyclization |
| format_facet |
Aufsätze Gedruckte Aufsätze |
| format_main_str_mv |
Text Zeitschrift/Artikel |
| carriertype_str_mv |
nc |
| hierarchy_parent_title |
Chinese journal of polymer science |
| hierarchy_parent_id |
130996939 |
| dewey-tens |
540 - Chemistry 660 - Chemical engineering 670 - Manufacturing |
| hierarchy_top_title |
Chinese journal of polymer science |
| isfreeaccess_txt |
false |
| familylinks_str_mv |
(DE-627)130996939 (DE-600)1082856-4 (DE-576)026374684 |
| title |
Palladium-catalyzed cycloaromatization polymerization of enediynes |
| ctrlnum |
(DE-627)OLC2038273499 (DE-He213)s10118-018-2088-9-p |
| title_full |
Palladium-catalyzed cycloaromatization polymerization of enediynes |
| author_sort |
Wang, Chonggang |
| journal |
Chinese journal of polymer science |
| journalStr |
Chinese journal of polymer science |
| lang_code |
eng |
| isOA_bool |
false |
| dewey-hundreds |
500 - Science 600 - Technology |
| recordtype |
marc |
| publishDateSort |
2017 |
| contenttype_str_mv |
txt |
| container_start_page |
237 |
| author_browse |
Wang, Chonggang Chen, Shudan Zhou, Hao Gu, Jinlou Hu, Aiguo |
| container_volume |
36 |
| class |
540 660 VZ 660 670 VZ |
| format_se |
Aufsätze |
| author-letter |
Wang, Chonggang |
| doi_str_mv |
10.1007/s10118-018-2088-9 |
| dewey-full |
540 660 670 |
| title_sort |
palladium-catalyzed cycloaromatization polymerization of enediynes |
| title_auth |
Palladium-catalyzed cycloaromatization polymerization of enediynes |
| abstract |
Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
| abstractGer |
Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
| abstract_unstemmed |
Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields. © Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018 |
| collection_details |
GBV_USEFLAG_A SYSFLAG_A GBV_OLC SSG-OLC-TEC SSG-OLC-CHE GBV_ILN_70 GBV_ILN_267 GBV_ILN_2018 GBV_ILN_4277 |
| container_issue |
2 |
| title_short |
Palladium-catalyzed cycloaromatization polymerization of enediynes |
| url |
https://doi.org/10.1007/s10118-018-2088-9 |
| remote_bool |
false |
| author2 |
Chen, Shudan Zhou, Hao Gu, Jinlou Hu, Aiguo |
| author2Str |
Chen, Shudan Zhou, Hao Gu, Jinlou Hu, Aiguo |
| ppnlink |
130996939 |
| mediatype_str_mv |
n |
| isOA_txt |
false |
| hochschulschrift_bool |
false |
| doi_str |
10.1007/s10118-018-2088-9 |
| up_date |
2024-07-03T18:14:09.135Z |
| _version_ |
1803582648232181760 |
| 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">OLC2038273499</controlfield><controlfield tag="003">DE-627</controlfield><controlfield tag="005">20230502172819.0</controlfield><controlfield tag="007">tu</controlfield><controlfield tag="008">200820s2017 xx ||||| 00| ||eng c</controlfield><datafield tag="024" ind1="7" ind2=" "><subfield code="a">10.1007/s10118-018-2088-9</subfield><subfield code="2">doi</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-627)OLC2038273499</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-He213)s10118-018-2088-9-p</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="4"><subfield code="a">540</subfield><subfield code="a">660</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="082" ind1="0" ind2="4"><subfield code="a">660</subfield><subfield code="a">670</subfield><subfield code="q">VZ</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Wang, Chonggang</subfield><subfield code="e">verfasserin</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Palladium-catalyzed cycloaromatization polymerization of enediynes</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="c">2017</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">Text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">ohne Hilfsmittel zu benutzen</subfield><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">Band</subfield><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="500" ind1=" " ind2=" "><subfield code="a">© Chinese Chemical Society, Institute of Chemistry, Chinese Academy of Sciences and Springer-Verlag GmbH Germany, part of Springer Nature 2018</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">Abstract Bergman cyclization has shown great promise in constructing conjugated polymers. However, the application of this reaction in polymer science is still limited due to the harsh reaction condition and ill-defined structure of the achieved polymers. To this end, the cycloaromatization polymerization of enediynes catalyzed by a series of transition metal catalysts is investigated in this work, by taking advantage of the coordination chemistry of the enediyne with the transition metal complexes. According to the nuclear magnetic resonance (NMR), Fourier transform infrared (FTIR), ultraviolet-visble (UV-Vis) spectroscopies and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS) analysis, the cycloaromatization polymerization of enediynes proceeds under milder conditions and in a more controlled manner in the presence of palladium(II) complexes, giving structurally regulated conjugated polymers in high yields.</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Transition metal catalysis</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Enediyne</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Polymerization</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Cycloaromatization</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Bergman cyclization</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Chen, Shudan</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Zhou, Hao</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Gu, Jinlou</subfield><subfield code="4">aut</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Hu, Aiguo</subfield><subfield code="4">aut</subfield></datafield><datafield tag="773" ind1="0" ind2="8"><subfield code="i">Enthalten in</subfield><subfield code="t">Chinese journal of polymer science</subfield><subfield code="d">Chinese Chemical Society and Institute of Chemistry, CAS, 1985</subfield><subfield code="g">36(2017), 2 vom: 01. Dez., Seite 237-243</subfield><subfield code="w">(DE-627)130996939</subfield><subfield code="w">(DE-600)1082856-4</subfield><subfield code="w">(DE-576)026374684</subfield><subfield code="x">0256-7679</subfield><subfield code="7">nnns</subfield></datafield><datafield tag="773" ind1="1" ind2="8"><subfield code="g">volume:36</subfield><subfield code="g">year:2017</subfield><subfield code="g">number:2</subfield><subfield code="g">day:01</subfield><subfield code="g">month:12</subfield><subfield code="g">pages:237-243</subfield></datafield><datafield tag="856" ind1="4" ind2="1"><subfield code="u">https://doi.org/10.1007/s10118-018-2088-9</subfield><subfield code="z">lizenzpflichtig</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_USEFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SYSFLAG_A</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_OLC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-TEC</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">SSG-OLC-CHE</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_70</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_267</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_2018</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">GBV_ILN_4277</subfield></datafield><datafield tag="951" ind1=" " ind2=" "><subfield code="a">AR</subfield></datafield><datafield tag="952" ind1=" " ind2=" "><subfield code="d">36</subfield><subfield code="j">2017</subfield><subfield code="e">2</subfield><subfield code="b">01</subfield><subfield code="c">12</subfield><subfield code="h">237-243</subfield></datafield></record></collection>
|
| score |
7.399479 |