[1] |
Kolb H C, Finn M G, Sharpless K B . Click chemistry: diverse chemical function from a few good reactions[J]. Angewandte Chemie International Edition, 2001,40:2004-2021.
doi: 10.1002/1521-3773(20010601)40:11<2004::aid-anie2004>3.3.co;2-x
pmid: 11433435
|
[2] |
张涛, 郑朝晖, 成煦 , 等. 材料科学中的点击化学[J]. 化学进展, 2008,20(7/8):1091-1101.
|
[3] |
Yu B, Justin W C, Charles E H , et al. Sequential thiol-ene/thiol-ene and thiol-ene/thiol-yne reactions as a route to well-defined mono and bis end-functionalized poly (N-isopropylacrylamide)[J]. Journal of Polymer Science. Part A: Polymer Chemistry, 2009,47:3544-3557.
doi: 10.1002/pola.v47:14
|
[4] |
Pounder R J, Stanford M J, Brooks P , et al. Metal free thiol-maleimide ``Click'' reaction as a mild functionalization strategy for degradable polymers[J]. Chemical Communications, 2008,41:5158-5160.
|
[5] |
Lutz J F, B$\acute{o}$rner H G, Weichenhan K. Combining ATRP and ``Click'' chemistry: a promising platform toward functional biocompatible polymers and polymer bioconjugates[J]. Macromolecules, 2006,39:6376-6383.
doi: 10.1021/ma061557n
|
[6] |
Harvison M A, Lowe A B . Nucleophile-initiated thiol-michael reactions: effect of organocatalyst, thiol, and ene[J]. Macromolecules Rapid Communications, 2011,32:779-800.
|
[7] |
Alessandro D . The emergence of thiol-ene coupling as a click process for materials and bioorganic chemistry[J]. Angewandte Chemie International Edition, 2008,47:2-5.
doi: 10.1002/(ISSN)1521-3773
|
[8] |
Killops K L, Campos L M, Hawker C J . Robust, efficient, and orthogonal synjournal of dendrimers via thiol-ene ``Click'' chemistry[J]. Journal of the American Chemical Society, 2008,130:5062-5064.
doi: 10.1021/ja8006325
pmid: 18355008
|
[9] |
Altintas O, Hizal G, Tunca U . ABC-type hetero-arm star terpolymers through "Click" chemistry[J]. Journal of Polymer Science. Part A: Polymer Chemistry, 2006,44:5699-5707.
doi: 10.1002/(ISSN)1099-0518
|
[10] |
Otsuka H, Nagano S, Kobashi Y , et al. A dynamic covalent polymer driven by disulfide metajournal under photoirradiation[J]. Chemical Communications, 2010,46:1150-1152.
doi: 10.1039/b916128g
pmid: 20126743
|
[11] |
Chan J W, Hoyle C E, Lowe A B , et al. Nucleophile-initiated thiol-michael reactions: effect of organocatalyst, thiol, and ene[J]. Macromolecules, 2010,43:6381-6388.
doi: 10.1021/ma101069c
|
[12] |
Lalev$\acute{e}$e J, Fabrice M S, Mohamad E R , et al. Thiyl radical generation in thiol or disulfide containing photosensitive systems[J]. Macromolecular Chemistry and Physics, 2010,211(1):103-110.
doi: 10.1002/macp.200900442
|
[13] |
Hoyle C E, Lee T Y, Roper T . Thiol-enes: chemistry of the past with promise for the future[J]. Journal of Polymer Science. Part A: Polymer Chemistry, 2004,42:5301-5338.
doi: 10.1002/(ISSN)1099-0518
|
[14] |
Hoyle C E, Bowman C N . Thiol-ene click chemistry[J]. Angewandte Chemie International Edition, 2010,49:1540-1573.
doi: 10.1002/anie.200903924
pmid: 20166107
|
[15] |
Campos L M, Meinel I, Guino R G , et al. Highly versatile and robust materials for soft imprint lithography based on thiol-ene click chemistry[J]. Advanced Materials, 2008,20:1-6.
|
[16] |
Uygun M, Tasdelen M A, Yagci Y . Influence of type of initiation on thiol-ene ``Click'' chemistry[J]. Macromolecular Chemistry and Physics, 2010,211(1):103-110.
doi: 10.1002/macp.200900442
|