Cucurbit[n]uril based supramolecular assemblies: tunable physico-chemical properties and their prospects

被引:162
|
作者
Bhasikuttan, Achikanath C. [1 ]
Pal, Haridas [1 ]
Mohanty, Jyotirmayee [1 ]
机构
[1] Bhabha Atom Res Ctr, Radiat & Photochem Div, Bombay 400085, Maharashtra, India
关键词
HOST-GUEST COMPLEXATION; THIOFLAVIN-T; FLUORESCENT DYES; CUCURBITURIL HOMOLOGS; PK(A) SHIFTS; ORGANIC-DYE; BINDING; ENCAPSULATION; EMISSION; DERIVATIVES;
D O I
10.1039/c1cc12091c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This Feature Article provides an account of the recent work by our research group (with some reference to relevant work of other groups) on the spectacular physico-chemical properties of cucurbituril-based supramolecular assemblies of chromophoric dyes having technological and biological importance. Simultaneous association of multiple hosts or guests either by cooperative binding or competitive displacement is an applied strategy to construct novel functional assemblies with predesignated characteristics. Here, effort has been made to briefly discuss the diverse photophysical characteristics of several host-guest complexes and the dynamic responses of such molecular assemblies towards external stimulants like metal ions. The detailed experimentation on these assemblies project their applications in the controlled uptake and release of drugs, photofunctional devices, aqueous-based dye lasers, and molecular architectures.
引用
收藏
页码:9959 / 9971
页数:13
相关论文
共 50 条
  • [31] Self-Assemblies Based on the "Outer-Surface Interactions" of Cucurbit[n]urils: New Opportunities for Supramolecular Architectures and Materials
    Ni, Xin-Long
    Xiao, Xin
    Cong, Hang
    Zhu, Qian-Jiang
    Xue, Sai-Feng
    Tao, Zhu
    ACCOUNTS OF CHEMICAL RESEARCH, 2014, 47 (04) : 1386 - 1395
  • [32] Coordination and Supramolecular Self-Assemblies of Alkali and Alkaline Earth Metal Ions to Cucurbit[5]uril in the Presence of Nitrophenol
    Chen, Kai
    Feng, Xing
    Liang, Li-Li
    Zhang, Yun-Qian
    Zhu, Qian-Jiang
    Xue, Sai-Feng
    Tao, Zhu
    CRYSTAL GROWTH & DESIGN, 2011, 11 (12) : 5712 - 5722
  • [33] Supramolecular Fluorescence Probe Based on Twisted Cucurbit[14]uril for Sensing Fungicide Flusilazole
    Fan, Ying
    Gao, Rui-Han
    Huang, Ying
    Bian, Bing
    Tao, Zhu
    Xiao, Xin
    FRONTIERS IN CHEMISTRY, 2019, 7
  • [34] Quantum-chemical study of the formation mechanism of cucurbit[n]uril nanocavitands
    Grishaeva, T. N.
    Maslii, A. N.
    Bakovets, V. V.
    Kuznetsov, An. M.
    RUSSIAN JOURNAL OF INORGANIC CHEMISTRY, 2010, 55 (10) : 1594 - 1599
  • [35] Density Functional Investigations on the Charge Distribution, Vibrational Spectra, and NMR Chemical Shifts in Cucurbit[n]uril (n=5-12) Hosts
    Gobre, Vivekanand V.
    Pinjari, Rahul V.
    Gejji, Shridhar P.
    JOURNAL OF PHYSICAL CHEMISTRY A, 2010, 114 (12) : 4464 - 4470
  • [36] A Ternary Supramolecular Self-Assembly Model Based on Cyclopentano Cucurbit[5]uril
    Wang, C.
    Cheng, S. Y.
    Zhao, W. W.
    Yang, X. N.
    Zhou, K. Z.
    Tian, J. J.
    Jiang, D. F.
    Ma, P. H.
    CRYSTALLOGRAPHY REPORTS, 2020, 65 (07) : 1156 - 1160
  • [37] Interaction of Phenyl-Substituted Diazaperylenium with Cucurbit[n]uril: Complex versus Supramolecular Polymer
    Thangavel, Arumugam
    Macias, Monica
    Tsumaki, Samantha
    ACS OMEGA, 2020, 5 (10): : 5574 - 5579
  • [38] Supramolecular tandem assay for tyrosinase based on cucurbit[8]uril induced peptide inclusion
    Cai, Yong-Qi
    Li, Gao
    DYES AND PIGMENTS, 2021, 195
  • [39] Synthesis and physico-chemical properties of a novel series of aromatic electron acceptors based on N-heterocycles
    Furdui, Bianca
    Dinica, Rodica M.
    Tabacaru, Aurel
    Pettinari, Claudio
    TETRAHEDRON, 2012, 68 (31) : 6164 - 6168
  • [40] Cucurbit[10]uril-Based [2]Rotaxane: Preparation and Supramolecular Assembly-Induced Fluorescence Enhancement
    Yu, Yang
    Li, Yawen
    Wang, Xiaoqing
    Nian, Hao
    Wang, Le
    Li, Jie
    Zhao, Yanxia
    Yang, Xiran
    Liu, Simin
    Cao, Liping
    JOURNAL OF ORGANIC CHEMISTRY, 2017, 82 (11) : 5590 - 5596