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Ring-Opening Polymerization of ε‑Caprolactone by Using Alum..:

Someswara Rao Kosuru (11090196) ; Yu-Lun Chang (1405921) ; Po-Yu Chen (706337)...
https://figshare.com/articles/journal_contribution/Ring-Opening_Polymerization_of_Caprolactone_by_Using_Aluminum_Complexes_Bearing_Aryl_Thioether_Phenolates_Labile_Thioether_Chelation/18290085. , 2022

Link: https://doi.org/10.1021/acs.inorgchem.1c03683.s002

RT Journal
T1 <Title>Ring-Opening Polymerization of ε‑Caprolactone by Using Aluminum Complexes Bearing Aryl Thioether Phenolates: Labile Thioether Chelation</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_18290085&Exemplar=1&LAN=DE
				
A1 Someswara Rao Kosuru (11090196)
A1 Yu-Lun Chang (1405921)
A1 Po-Yu Chen (706337)
A1 Wei Lee (3978110)
A1 Yi-Chun Lai (451251)
A1 Shangwu Ding (1953664)
A1 Hsuan-Ying Chen (510813)
A1 Hsing-Yin Chen (1405912)
A1 Yung-Chi Chang (216307)
YR 2022
K1 Biochemistry
K1 Molecular Biology
K1 Physiology
K1 Sociology
K1 Environmental Sciences not elsewhere classified
K1 Biological Sciences not elsewhere classified
K1 Chemical Sciences not elsewhere classified
K1 electron deficiency substituents
K1 thioether coordination stabilized
K1 suitable chelating group
K1 ts1 </ b
K1 alme </ b
K1 labile thioether chelation
K1 higher activation energy
K1 cl polymerization rate
K1 cl polymerization due
K1 ε ‑ caprolactone
K1 thioether group
K1 labile nature
K1 opening polymerization
K1 reduced form
K1 phenolate decreased
K1 oxidized form
K1 catalytic activity
K1 arylthiomethylphenolate ligands
K1 al complexes
K1 al catalysts
K1 97 %)
K1 75 min
K1 60 min
K1 45 %)
K1 4320 min
K1 40 min
K1 100 %)
JF https://figshare.com/articles/journal_contribution/Ring-Opening_Polymerization_of_Caprolactone_by_Using_Aluminum_Complexes_Bearing_Aryl_Thioether_Phenolates_Labile_Thioether_Chelation/18290085
LK http://dx.doi.org/https://doi.org/10.1021/acs.inorgchem.1c03683.s002
DO https://doi.org/10.1021/acs.inorgchem.1c03683.s002
SF ELIB - SuUB Bremen

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