Metal-free click approach for facile production of main chain poly(bile acid)s
Literature Information
Tian Tian, Wei Zhu, Jiecheng Cui, Yong Ju, Guangtao Li
In this work, a metal-free click polymerization approach was developed to facilely produce versatile main chain poly(bile acid)s with high efficiency. No metal catalysts and organic solvents are required for the polymerization process, which exhibits multiple advantages, including less toxicity, being environmentally friendly and economically sound. Remarkably, the polymerization can finish within several minutes when the reactive monomers are in a crystalline state. Although the monomers are amorphous, no more than one hour is needed for completing the polymerization. The conversion efficiency can reach up to nearly 100% with the polymer molecular weight up to 93 500 Da, which still shows good solubility in most common solvents. The described approach is applicable for various bile acid monomers with different linkages, including long flexible alkyl chains, amide groups, phenyl groups and sterically hindered structures. Probably due to the strengthened hydrogen bonding interactions, π–π stacking and the hindrance effect introduced by the linkage used, the molecular weight and properties of the resulting polymers are strongly dependent on the monomer structures. Notably, by introducing a steric effect on azide groups (4e and 4f), the regioselectivity of the 1,4-triazole linkers is significantly improved from 60% to 85%. All the obtained polymers are thermally stable and display high resistance to thermal degradation.
Related Literature
Synthesis and reactivity of triethylborane adduct of N-heterocyclic carbene: versatile synthons for synthesis of N-heterocyclic carbene complexes
Yoshitaka Yamaguchi, Taigo Kashiwabara, Kenichi Ogata, Yumiko Miura, Yoshiyuki Nakamura, Kimiko Kobayashi, Takashi Ito
DOI: 10.1039/B405459H
Aminooxazolinate; a chiral amidinate analogue
Ian J. Munslow, Andrew R. Wade, Robert J. Deeth, Peter Scott
DOI: 10.1039/B409113B
Highly efficient epoxidation method of olefins with hydrogen peroxide as terminal oxidant, bicarbonate as a co-catalyst and oxodiperoxo molybdenum(vi) complex as catalyst
Narottam Gharah, Santu Chakraborty, Alok K. Mukherjee, Ramgopal Bhattacharyya
DOI: 10.1039/B408946D
A thermally stable nanoporous nickel 5-sulfoisophthalate; crystal structure and adsorption properties
Dae Sung Kim, Paul M. Forster, Ronan Le Toquin, Anthony K. Cheetham
DOI: 10.1039/B408535C
High efficiency mer-iridium complexes for organic light-emitting diodes
Cheng-Hsien Yang, Kai-Hung Fang, Chun-Hung Chen, I-Wen Sun
DOI: 10.1039/B406958G
Synthesis and electropolymerization of novel oligothiophene-functionalized perylene bisimides
Chang-Cheng You, Chantu R. Saha-Möller, Frank Würthner
DOI: 10.1039/B407551J
A regioregular polyalkylthiophene bearing covalently-linked biotin, and its interaction with avidin in solution and in thin films
Fouzi Mouffouk, Simon J. Higgins, Stewart J. Brown, Naser Sedghi, Bill Eccleston, Stuart Reeman
DOI: 10.1039/B408935A
Novel fullerene–porphyrin–fullerene triad linked by metal axial coordination: Synthesis, X-ray crystal structure, and spectroscopic characterizations of trans-bis([60]fullerenoacetato)tin(iv) porphyrin
Hyun Jung Kim, Ki-Min Park, Seong Keun Kim, Kil Suk Kim, Dongho Kim, Hee-Joon Kim
DOI: 10.1039/B411482E
Facile deposition of copper-doped diamond-like carbon nanocomposite films by a liquid-phase electrochemical route
Heqing Jiang, Lina Huang, Zhijun Zhang, Tao Xu, Weimin Liu
DOI: 10.1039/B408497G
Secondary coordination sphere controlled reversible geometry reorganisations in copper(ii) complexes
John Fielden, De-Liang Long, Leroy Cronin
DOI: 10.1039/B407229D
You might also like
What is 1-(2,4,6-Trifluorophenyl)ethanol (CAS: 1250113-83-7)?
1-(2,4,6-Trifluorophenyl)ethanol is an organic compound with the CAS number 1250...
Is 1-(2,4-Dimethoxybenzyl)-4-(hydroxymethyl)-2-pyrrolidinone (CAS: 919111-34-5) safe?
1-(2,4-Dimethoxybenzyl)-4-(hydroxymethyl)-2-pyrrolidinone (CAS: 919111-34-5) is ...
What are the physical and chemical properties of (7S,15R)-6β,15-Diacetoxy-7α,20-epoxy-7-hydroxykaura-2,16-dien-1-one (CAS: 51419-51-3)?
(7S,15R)-6β,15-Diacetoxy-7α,20-epoxy-7-hydroxykaura-2,16-dien-1-one is a crystal...
What regulatory guidelines apply to rac-ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate, trans (CAS: 3618-04-0)?
The compound rac-ethyl (1r,4r)-4-hydroxycyclohexane-1-carboxylate, trans (CAS: 3...
What is the market or research trend for 2-(2,4-Difluorophenoxy)-3-nitropyridine (CAS: 175135-62-3)?
The market for 2-(2,4-Difluorophenoxy)-3-nitropyridine (CAS: 175135-62-3) is cur...
What are the main uses of 6-Diazo-5-oxo-L-norleucine (CAS: 157-03-9)?
The main uses of 6-Diazo-5-oxo-L-norleucine (CAS: 157-03-9) include research in ...
What precautions should be taken when handling 2-Aminoethyl-mono-amide-DOTA-tris(tBu ester) (CAS: 173308-19-5)?
When handling 2-Aminoethyl-mono-amide-DOTA-tris(tBu ester) (CAS: 173308-19-5), i...
How is 5-Methylimidazo[1,2-a]pyridine-3-carbaldehyde (CAS: 178488-37-4) typically synthesized?
5-Methylimidazo[1,2-a]pyridine-3-carbaldehyde (CAS: 178488-37-4) can be synthesi...
Are there alternatives to 2,4,6-Trihydroxyisophthalaldehyde (CAS: 4396-13-8) in synthesis?
There are alternative reagents that can be used in the synthesis of 2,4,6-Trihyd...
What is (2Z)-3-(5-Fluoro-1H-indol-3-yl)-2-sulfanylacrylic acid (CAS: 179461-52-0)?
(2Z)-3-(5-Fluoro-1H-indol-3-yl)-2-sulfanylacrylic acid is a chemical compound wi...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.














