4.7 Article

Carborane RAFT agents as tunable and functional molecular probes for polymer materials

Journal

POLYMER CHEMISTRY
Volume 10, Issue 13, Pages 1660-1667

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9py00199a

Keywords

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Funding

  1. UCLA Department of Chemistry and Biochemistry
  2. NSF [HRD-1400789, DGE-0707424, CHE-1507735, CHE-1552849]
  3. UCLA
  4. Gold Family Foundation
  5. SPE Foundation

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Functional handles appended to polymer chain ends are important tools often used as spectroscopic probes for determining polymer structure, affinity labels, and as reactive handles for the conjugation of functional payloads. An easily tunable molecular handle able to carry out multiple functions simultaneously would be of significant use at the polymer, materials, and biology interface. Here, we report the development of carborane-containing chain transfer agents (CTAs, commonly referred to as RAFT agents) which are used in reversible addition-fragmentation chain transfer (RAFT) polymerization. These carborane RAFT agents establish control over polymerization processes leading to monodisperse (D = 1.03-1.15) polymers made from N-isopropylacrylamide, styrene, 4-chlorostyrene, and methyl acrylate monomers. The tunable nature of the carborane-based scaffold appended on the polymer chain end serves as a general H-1 NMR spectroscopic handle, which can be used to elucidate polymer molecular weight via end-group analysis. Isothermal titration calorimetry (ITC) measurements show that synthesized carborane terminated polymers exhibit strong binding to beta-cyclodextrin with an affinity (K-a) of 9.37 x 10(4) M-1, thereby demonstrating its potential use as an affinity label. Additionally, we show that the free B-H vertices on the carborane RAFT agents exhibit a Raman vibrational signal at similar to 2549 cm(-1), a Ramansilent region for biological milieu, indicating its potential utility as an innate Raman active probe. The reported carborane RAFT agents bolster the expanding toolbox of molecular probes and serve as tunable platforms for incorporating additional and complementary handles for tailoring chain-end functionality and facilitating polymer analysis.

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