Issue 47, 2014

Multi-responsive cellulose nanocrystal–rhodamine conjugates: an advanced structure study by solid-state dynamic nuclear polarization (DNP) NMR

Abstract

Multi-stimuli responsive materials based on cellulose nanocrystals (CNCs), especially using non-conventional stimuli including light, still need more explorations, to fulfill the requirements of complicated application environments. The structure determination of functional groups on the CNC surface constitutes a significant challenge, partially due to their low amounts. In this study, rhodamine spiroamide groups are immobilized onto the surface of CNCs leading to a hybrid compound being responsive to pH-values, heat and UV light. After the treatment with external stimuli, the fluorescent and correlated optical color change can be induced, which refers to a ring opening and closing process. Amine and amide groups in rhodamine spiroamide play the critical role in this switching process. Solid-state NMR spectroscopy coupled with sensitivity-enhanced dynamic nuclear polarization (DNP) was used to measure 13C and 15N in natural abundance, allowing the determination of structural changes during the switching process. It is shown that a temporary bond through an electrostatic interaction could be formed within the confined environment on the CNC surface during the heat treatment. The carboxyl groups on the CNC surface play a pivotal role in stabilizing the open status of rhodamine spiroamide groups.

Graphical abstract: Multi-responsive cellulose nanocrystal–rhodamine conjugates: an advanced structure study by solid-state dynamic nuclear polarization (DNP) NMR

Supplementary files

Article information

Article type
Paper
Submitted
11 Sep 2014
Accepted
23 Oct 2014
First published
24 Oct 2014

Phys. Chem. Chem. Phys., 2014,16, 26322-26329

Author version available

Multi-responsive cellulose nanocrystal–rhodamine conjugates: an advanced structure study by solid-state dynamic nuclear polarization (DNP) NMR

L. Zhao, W. Li, A. Plog, Y. Xu, G. Buntkowsky, T. Gutmann and K. Zhang, Phys. Chem. Chem. Phys., 2014, 16, 26322 DOI: 10.1039/C4CP04096A

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