Polymer Functional Nanodiamonds by Light-Induced Ligation

Polymer Functional Nanodiamonds by Light-Induced Ligation
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DOI:
10.1021/acs.macromol.5b02607
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发表时间:
2016-02
期刊:
影响因子:
5.5
通讯作者:
Kilian N. R. Wuest;V. Trouillet;Anja S. Goldmann;M. Stenzel;C. Barner‐Kowollik
Kilian N. R. Wuest;V. Trouillet;Anja S. Goldmann;M. Stenzel;C. Barner‐Kowollik
中科院分区:
化学1区
文献类型:
--
作者:
Kilian N. R. Wuest;V. Trouillet;Anja S. Goldmann;M. Stenzel;C. Barner‐Kowollik

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A light-triggered strategy to functionalize nanodiamonds (NDs) with well-defined functional polymers is presented. The employed grafting approach is based on o-methylbenzaldehydes, which upon UV irradiation form o-quinodimethanes that undergo Diels–Alder reactions with dienophiles. A series of well-defined maleimide end-group functional polymers, i.e., poly(styrene) (Mn = 5800 g mol–1; Đ = 1.2), poly(N-isopropylacrylamide) (Mn = 5800 g mol–1, Đ = 1.2), and poly(2-(2′,3′,4′,6′-tetra-O-acetyl-α-d-mannosyloxy)ethyl methacrylate) (Mn = 24 300, 39 000, and 58 800 g mol–1, Đ ≤ 1.3), were prepared via reversible addition–fragmentation chain transfer (RAFT) polymerization of protected maleimide functional RAFT agents. After deprotection of the furan-protected maleimide end groups, the polymers were photografted to o-methylbenzaldehyde functional NDs and characterized in detail via infrared (IR) spectroscopy, X-ray photoelectron spectroscopy (XPS), and thermogravimetric analysis (TGA). The grafting density decreas...