Fast conversion of terminal thiocarbonylthio groups of RAFT polymers to “clickable” thiol groups via versatile sodium azide

Literature Information

Publication Date 2014-06-17
DOI 10.1039/C4PY00732H
Impact Factor 5.582
Authors

Yang Wu, Yanyan Zhou, Jian Zhu, Wei Zhang, Xiangqiang Pan, Zhengbiao Zhang, Xiulin Zhu


View Original

Abstract

This work reports a facile and fast way of removing thiocarbonylthio end groups of RAFT-made polymers by the utilization of sodium azide (NaN3) without deoxygenation. Within several minutes (1–5 minutes), the terminal thiocarbonylthio group of RAFT-made polybutylacrylate (PBA) was completely removed upon NaN3 treatment as revealed by nuclear magnetic resonance. Careful identification of the chain end structure of the resultant polymer was implemented by matrix-assisted laser desorption ionization time-of-flight mass spectrometry, and the results unambiguously proved that the terminal thiocarbonylthio group was converted to the “clickable” thiol group by NaN3via a nucleophilic process. Polystyrene, poly(methyl methacrylate) and poly(vinyl acetate) prepared by the RAFT technique with different kinds of RAFT agents have also been examined under identical conditions. Similar results were obtained, demonstrating a good universality of this approach. This work provides an alternative and effective approach for removing/modifying thiocarbonylthio end groups of RAFT-made polymers, while producing “clickable” thiol-terminated polymers for many post-modification possibilities.

Related Literature

Inside front cover

Cover

DOI: 10.1039/C9CP90241D

Effect of mild nanoscopic confinement on the dynamics of ionic liquids

Daria Noferini, Olaf Holderer, Henrich Frielinghaus

2020-04-09 Paper

DOI: 10.1039/C9CP05200C

Multi-conformational monomer and dimer steady-states in domains of a few molecules: the consequences on the phosphorescence emission bands

Gustavo H. R. Soares, Guilherme A. M. Jardim, Eufrânio N. da Silva Júnior, Luiz A. Cury

2019-09-16 Paper

DOI: 10.1039/C9CP04706A

Back cover

Cover

DOI: 10.1039/C9CP90251A

Molecular dynamics involving proton exchange of a protic ionic liquid–water mixture studied by NMR spectroscopy

Mohammad Hasani, Lars Nordstierna, Anna Martinelli

2019-09-17 Paper

DOI: 10.1039/C9CP03563J

Four resonance structures elucidate double-bond isomerisation of a biological chromophore

Evgeniy V. Gromov, Tatiana Domratcheva

2020-04-09 Paper

DOI: 10.1039/D0CP00814A

Understanding the properties of dithienylethenes functionalized for supramolecular self-assembly: a molecular modeling study

Laura Le Bras, Roxanne Berthin, Ismaïl Hamdi, Maroua Louati, Stéphane Aloïse, Michinori Takeshita

2020-03-09 Paper

DOI: 10.1039/C9CP06590C

Contents list

Front/Back Matter

DOI: 10.1039/C9CP90242B

Effect of graphene between photoanode and sensitizer on the intramolecular and intermolecular electron transfer process

Xiaofei Wang, Yuanzuo Li, Peng Song, Fengcai Ma, Yanhui Yang

2020-02-28 Paper

DOI: 10.1039/C9CP06543A

You might also like

Compound Q&A

What are the main uses of 4-Nitrophenyl phosphate disodium salt hexahydrate (CAS: 333338-18-4)?

4-Nitrophenyl phosphate disodium salt hexahydrate is primarily used as a substra...

333338-18-44-Nitrophenyl phosph...
Compound Q&A

What are the main uses of 2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4)?

2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4) is widely ...

1060816-01-42-(Trifluoromethyl)-...
Compound Q&A

How should 2-Fluoro-4-biphenylcarboxylic acid (CAS: 137045-30-8) be stored?

2-Fluoro-4-biphenylcarboxylic acid should be stored in a cool, dry place at room...

137045-30-82-Fluoro-4-biphenylc...
Compound Q&A

What industries use Prednisolone-21-Carboxylic Acid (CAS: 61549-70-0)?

Prednisolone-21-Carboxylic Acid is primarily used in the pharmaceutical industry...

61549-70-0Prednisolone-21-Carb...
Compound Q&A

How should 4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) be stored?

4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) should be stored in a co...

3614-72-04-(Hydrazinomethyl)-...
Compound Q&A

What industries use 4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8)?

4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8) i...

92534-70-84-Amino-1-methyl-1H-...
Compound Q&A

What regulatory guidelines apply to dehydropachymic acid (CAS: 77012-31-8)?

Dehydropachymic acid (CAS: 77012-31-8) is regulated by various agencies. It fall...

77012-31-8Dehydropachymic acid
Compound Q&A

What is the market or research trend for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic acid (CAS: 898561-66-5)?

The market and research trends for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic aci...

898561-66-56-[(2,2-Dimethylprop...
Compound Q&A

How should 1,10-Phenanthroline-2,9-dicarbaldehyde (CAS: 57709-62-3) be stored?

1,10-Phenanthroline-2,9-dicarbaldehyde should be stored in a cool, dry place awa...

57709-62-31,10-Phenanthroline-...
Compound Q&A

How is 5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate (CAS: 113952-21-9) typically synthesized?

5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate can be synt...

113952-21-95-Carbamoyl-11-oxo-1...

Source Journal

Polymer Chemistry

Polymer Chemistry
CiteScore: 8.6
Self-citation Rate: 7.3%
Articles per Year: 457

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.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.