A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides
Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoidin...
Ausführliche Beschreibung
Autor*in: |
Douka, Aliki [verfasserIn] |
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Format: |
E-Artikel |
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Sprache: |
Englisch |
Erschienen: |
2018transfer abstract |
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Schlagwörter: |
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Umfang: |
25 |
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Übergeordnetes Werk: |
Enthalten in: LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY - Ruff, Christian T. ELSEVIER, 2012, Amsterdam [u.a.] |
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Übergeordnetes Werk: |
volume:79 ; year:2018 ; pages:1-25 ; extent:25 |
Links: |
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DOI / URN: |
10.1016/j.progpolymsci.2017.10.001 |
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Katalog-ID: |
ELV042647991 |
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245 | 1 | 0 | |a A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides |
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520 | |a Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. | ||
520 | |a Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. | ||
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10.1016/j.progpolymsci.2017.10.001 doi GBV00000000000195A.pica (DE-627)ELV042647991 (ELSEVIER)S0079-6700(16)30085-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 600 690 VZ 51.00 bkl 51.32 bkl Douka, Aliki verfasserin aut A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides 2018transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE Elsevier Vouyiouka, Stamatina oth Papaspyridi, Lefki-Maria oth Papaspyrides, Constantine D. oth Enthalten in Elsevier Science Ruff, Christian T. ELSEVIER LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY 2012 Amsterdam [u.a.] (DE-627)ELV011160764 volume:79 year:2018 pages:1-25 extent:25 https://doi.org/10.1016/j.progpolymsci.2017.10.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_11 GBV_ILN_21 GBV_ILN_31 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_74 GBV_ILN_105 GBV_ILN_2010 GBV_ILN_2021 51.00 Werkstoffkunde: Allgemeines VZ 51.32 Werkstoffmechanik VZ AR 79 2018 1-25 25 045F 540 |
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10.1016/j.progpolymsci.2017.10.001 doi GBV00000000000195A.pica (DE-627)ELV042647991 (ELSEVIER)S0079-6700(16)30085-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 600 690 VZ 51.00 bkl 51.32 bkl Douka, Aliki verfasserin aut A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides 2018transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE Elsevier Vouyiouka, Stamatina oth Papaspyridi, Lefki-Maria oth Papaspyrides, Constantine D. oth Enthalten in Elsevier Science Ruff, Christian T. ELSEVIER LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY 2012 Amsterdam [u.a.] (DE-627)ELV011160764 volume:79 year:2018 pages:1-25 extent:25 https://doi.org/10.1016/j.progpolymsci.2017.10.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_11 GBV_ILN_21 GBV_ILN_31 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_74 GBV_ILN_105 GBV_ILN_2010 GBV_ILN_2021 51.00 Werkstoffkunde: Allgemeines VZ 51.32 Werkstoffmechanik VZ AR 79 2018 1-25 25 045F 540 |
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10.1016/j.progpolymsci.2017.10.001 doi GBV00000000000195A.pica (DE-627)ELV042647991 (ELSEVIER)S0079-6700(16)30085-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 600 690 VZ 51.00 bkl 51.32 bkl Douka, Aliki verfasserin aut A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides 2018transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE Elsevier Vouyiouka, Stamatina oth Papaspyridi, Lefki-Maria oth Papaspyrides, Constantine D. oth Enthalten in Elsevier Science Ruff, Christian T. ELSEVIER LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY 2012 Amsterdam [u.a.] (DE-627)ELV011160764 volume:79 year:2018 pages:1-25 extent:25 https://doi.org/10.1016/j.progpolymsci.2017.10.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_11 GBV_ILN_21 GBV_ILN_31 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_74 GBV_ILN_105 GBV_ILN_2010 GBV_ILN_2021 51.00 Werkstoffkunde: Allgemeines VZ 51.32 Werkstoffmechanik VZ AR 79 2018 1-25 25 045F 540 |
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10.1016/j.progpolymsci.2017.10.001 doi GBV00000000000195A.pica (DE-627)ELV042647991 (ELSEVIER)S0079-6700(16)30085-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 600 690 VZ 51.00 bkl 51.32 bkl Douka, Aliki verfasserin aut A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides 2018transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE Elsevier Vouyiouka, Stamatina oth Papaspyridi, Lefki-Maria oth Papaspyrides, Constantine D. oth Enthalten in Elsevier Science Ruff, Christian T. ELSEVIER LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY 2012 Amsterdam [u.a.] (DE-627)ELV011160764 volume:79 year:2018 pages:1-25 extent:25 https://doi.org/10.1016/j.progpolymsci.2017.10.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_11 GBV_ILN_21 GBV_ILN_31 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_74 GBV_ILN_105 GBV_ILN_2010 GBV_ILN_2021 51.00 Werkstoffkunde: Allgemeines VZ 51.32 Werkstoffmechanik VZ AR 79 2018 1-25 25 045F 540 |
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10.1016/j.progpolymsci.2017.10.001 doi GBV00000000000195A.pica (DE-627)ELV042647991 (ELSEVIER)S0079-6700(16)30085-5 DE-627 ger DE-627 rakwb eng 540 540 DE-600 610 VZ 600 690 VZ 51.00 bkl 51.32 bkl Douka, Aliki verfasserin aut A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides 2018transfer abstract 25 nicht spezifiziert zzz rdacontent nicht spezifiziert z rdamedia nicht spezifiziert zu rdacarrier Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE Elsevier Vouyiouka, Stamatina oth Papaspyridi, Lefki-Maria oth Papaspyrides, Constantine D. oth Enthalten in Elsevier Science Ruff, Christian T. ELSEVIER LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY 2012 Amsterdam [u.a.] (DE-627)ELV011160764 volume:79 year:2018 pages:1-25 extent:25 https://doi.org/10.1016/j.progpolymsci.2017.10.001 Volltext GBV_USEFLAG_U GBV_ELV SYSFLAG_U GBV_ILN_11 GBV_ILN_21 GBV_ILN_31 GBV_ILN_40 GBV_ILN_62 GBV_ILN_65 GBV_ILN_74 GBV_ILN_105 GBV_ILN_2010 GBV_ILN_2021 51.00 Werkstoffkunde: Allgemeines VZ 51.32 Werkstoffmechanik VZ AR 79 2018 1-25 25 045F 540 |
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Enthalten in LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY Amsterdam [u.a.] volume:79 year:2018 pages:1-25 extent:25 |
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Enthalten in LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY Amsterdam [u.a.] volume:79 year:2018 pages:1-25 extent:25 |
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Lipase CR CLL 1,4-CHDM Mw 1H NMR 8-OL DP Lipase CC PE 4.4 AYL IM-PC T m T g L-MA Lipase PF Lipase PC UDL Lipase PA PSA PBS [η] t-BuOH DADD ω-carboxyl SA scCO2 PA(s) ω-carboxyl OA MW N435 RSM PE(s) EAPC TGA EAM PSAII ILs Lipase A ROP Lipase G DLA PCL PEA(s) PTC ε-CL HLE LLA δ-VL HiC e-ROP FDCA PLA PHA CALB K PHB BDO DDL PPL PSAI SA Lipase MM HDL THF Lipase RM PDI T TSAS Lipase RJ OH PDL CLEA COOH PDO MWD T b Lipase RD ω-HA DEA Mn DBTO [C4mim][PF6] k SSP DAO DES PEG [C4mim][NTf2] PD [C4mim][BF4] 12-Me-DDL PEL GADE |
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LONG-TERM RISK AND PROGNOSIS OF RECURRENT CARDIOVASCULAR EVENTS IN THE REACH REGISTRY |
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Douka, Aliki @@aut@@ Vouyiouka, Stamatina @@oth@@ Papaspyridi, Lefki-Maria @@oth@@ Papaspyrides, Constantine D. @@oth@@ |
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540 540 DE-600 610 VZ 600 690 VZ 51.00 bkl 51.32 bkl A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE Elsevier |
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ddc 540 ddc 610 ddc 600 bkl 51.00 bkl 51.32 Elsevier Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE |
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ddc 540 ddc 610 ddc 600 bkl 51.00 bkl 51.32 Elsevier Lipase CR Elsevier CLL Elsevier 1,4-CHDM Elsevier Mw Elsevier 1H NMR Elsevier 8-OL Elsevier DP Elsevier Lipase CC Elsevier PE 4.4 Elsevier AYL Elsevier IM-PC Elsevier T m Elsevier T g Elsevier L-MA Elsevier Lipase PF Elsevier Lipase PC Elsevier UDL Elsevier Lipase PA Elsevier PSA Elsevier PBS Elsevier [η] Elsevier t-BuOH Elsevier DADD Elsevier ω-carboxyl SA Elsevier scCO2 Elsevier PA(s) Elsevier ω-carboxyl OA Elsevier MW Elsevier N435 Elsevier RSM Elsevier PE(s) Elsevier EAPC Elsevier TGA Elsevier EAM Elsevier PSAII Elsevier ILs Elsevier Lipase A Elsevier ROP Elsevier Lipase G Elsevier DLA Elsevier PCL Elsevier PEA(s) Elsevier PTC Elsevier ε-CL Elsevier HLE Elsevier LLA Elsevier δ-VL Elsevier HiC Elsevier e-ROP FDCA Elsevier PLA Elsevier PHA Elsevier CALB Elsevier K Elsevier PHB Elsevier BDO Elsevier DDL Elsevier PPL Elsevier PSAI Elsevier SA Elsevier Lipase MM Elsevier HDL Elsevier THF Elsevier Lipase RM Elsevier PDI Elsevier T Elsevier TSAS Elsevier Lipase RJ Elsevier OH Elsevier PDL Elsevier CLEA Elsevier COOH Elsevier PDO Elsevier MWD Elsevier T b Elsevier Lipase RD Elsevier ω-HA Elsevier DEA Elsevier Mn Elsevier DBTO Elsevier [C4mim][PF6] Elsevier k Elsevier SSP Elsevier DAO Elsevier DES Elsevier PEG Elsevier [C4mim][NTf2] Elsevier PD Elsevier [C4mim][BF4] Elsevier 12-Me-DDL Elsevier PEL Elsevier GADE |
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A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides |
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a review on enzymatic polymerization to produce polycondensation polymers: the case of aliphatic polyesters, polyamides and polyesteramides |
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A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides |
abstract |
Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. |
abstractGer |
Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. |
abstract_unstemmed |
Enzymatic polymerization represents today an effective and preferable alternative to conventional chemically-catalyzed processes. It offers significant advantages, summarized in the applied mild reaction conditions mainly in terms of temperature and toxicity, and high selectivity of enzymes, avoiding protection-deprotection strategies and resulting in improved quality/performance of end products. Especially for polycondensation polymers, biocatalyzed synthetic routes have been under research for the last thirty years, including homo- and copolymerization of a significant number of monomers. Aliphatic polyesters, polyamides and at a much lower extent polyesteramides, represent the core of the pertinent studies, and are systematically discussed in the current review. Emphasis is given on polycondensates with biodegradability properties, derived from bio-based monomers such as succinic acid, 1,3- propanediol and lactide/lactic acid. |
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title_short |
A review on enzymatic polymerization to produce polycondensation polymers: The case of aliphatic polyesters, polyamides and polyesteramides |
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