A versatile new monomer family: Functionalized 4-vinyl-1,2,3-triazoles via click chemistry

Raymond J. Thibault; Kenichi Takizawa; Peter Lowenheilm; Brett Helms; Justin L. Mynar; Jean M.J. Fréchet; Craig J. Hawker

doi:10.1021/ja0648209

A versatile new monomer family: Functionalized 4-vinyl-1,2,3-triazoles via click chemistry

Raymond J. Thibault, Kenichi Takizawa, Peter Lowenheilm, Brett Helms, Justin L. Mynar, Jean M.J. Fréchet, Craig J. Hawker^*

^*Corresponding author for this work

Research output: Contribution to journal › Article › peer-review

170 Scopus citations

Abstract

Using facile, highly modular synthetic approaches, a new monomer family based on a 1,2,3-triazole-4-vinyl building block has been prepared, and various functional derivatives have been obtained. Subsequent homo- and copolymerization of these novel functionalized monomers gives polymeric materials with unique physical properties, combining many attractive features of more traditional monomers, such as styrene, vinylpyridine, and meth/acrylates.

Original language	English (US)
Pages (from-to)	12084-12085
Number of pages	2
Journal	Journal of the American Chemical Society
Volume	128
Issue number	37
DOIs	https://doi.org/10.1021/ja0648209
State	Published - Sep 20 2006
Externally published	Yes

ASJC Scopus subject areas

Catalysis
General Chemistry
Biochemistry
Colloid and Surface Chemistry

Access to Document

10.1021/ja0648209

Cite this

@article{12b4e7eba3f94825a6191c6cdf123118,

title = "A versatile new monomer family: Functionalized 4-vinyl-1,2,3-triazoles via click chemistry",

abstract = "Using facile, highly modular synthetic approaches, a new monomer family based on a 1,2,3-triazole-4-vinyl building block has been prepared, and various functional derivatives have been obtained. Subsequent homo- and copolymerization of these novel functionalized monomers gives polymeric materials with unique physical properties, combining many attractive features of more traditional monomers, such as styrene, vinylpyridine, and meth/acrylates.",

author = "Thibault, {Raymond J.} and Kenichi Takizawa and Peter Lowenheilm and Brett Helms and Mynar, {Justin L.} and Fr{\'e}chet, {Jean M.J.} and Hawker, {Craig J.}",

year = "2006",

month = sep,

day = "20",

doi = "10.1021/ja0648209",

language = "English (US)",

volume = "128",

pages = "12084--12085",

journal = "Journal of the American Chemical Society",

issn = "0002-7863",

publisher = "American Chemical Society",

number = "37",

}

TY - JOUR

T1 - A versatile new monomer family

T2 - Functionalized 4-vinyl-1,2,3-triazoles via click chemistry

AU - Thibault, Raymond J.

AU - Takizawa, Kenichi

AU - Lowenheilm, Peter

AU - Helms, Brett

AU - Mynar, Justin L.

AU - Fréchet, Jean M.J.

AU - Hawker, Craig J.

PY - 2006/9/20

Y1 - 2006/9/20

N2 - Using facile, highly modular synthetic approaches, a new monomer family based on a 1,2,3-triazole-4-vinyl building block has been prepared, and various functional derivatives have been obtained. Subsequent homo- and copolymerization of these novel functionalized monomers gives polymeric materials with unique physical properties, combining many attractive features of more traditional monomers, such as styrene, vinylpyridine, and meth/acrylates.

AB - Using facile, highly modular synthetic approaches, a new monomer family based on a 1,2,3-triazole-4-vinyl building block has been prepared, and various functional derivatives have been obtained. Subsequent homo- and copolymerization of these novel functionalized monomers gives polymeric materials with unique physical properties, combining many attractive features of more traditional monomers, such as styrene, vinylpyridine, and meth/acrylates.

UR - http://www.scopus.com/inward/record.url?scp=33748773913&partnerID=8YFLogxK

U2 - 10.1021/ja0648209

DO - 10.1021/ja0648209

M3 - Article

C2 - 16967955

AN - SCOPUS:33748773913

SN - 0002-7863

VL - 128

SP - 12084

EP - 12085

JO - Journal of the American Chemical Society

JF - Journal of the American Chemical Society

IS - 37

ER -

A versatile new monomer family: Functionalized 4-vinyl-1,2,3-triazoles via click chemistry

Abstract

ASJC Scopus subject areas

Access to Document

Other files and links

Fingerprint

Cite this