Assembly and applications of macrocyclic-confinement-derived supramolecular organic luminescent emissions from cucurbiturils
H Nie, Z Wei, XL Ni, Y Liu - Chemical Reviews, 2022 - ACS Publications
Cucurbit [n] urils (Q [n] s or CB [n] s), as a classical of artificial organic macrocyclic hosts,
were found to have excellent advantages in the fabricating of tunable and smart organic …
were found to have excellent advantages in the fabricating of tunable and smart organic …
Stimuli-responsive mechanically interlocked molecules constructed from cucurbit [n] uril homologues and derivatives
JX Liu, K Chen, C Redshaw - Chemical Society Reviews, 2023 - pubs.rsc.org
Cucurbit [n] uril supramolecular chemistry has developed rapidly since 2001 when different
cucurbit [n] uril homologues (Q [n]) were successfully separated in pure form. The …
cucurbit [n] uril homologues (Q [n]) were successfully separated in pure form. The …
[HTML][HTML] Artificial molecular machines
The widespread use of molecular machines in biology has long suggested that great
rewards could come from bridging the gap between synthetic molecular systems and the …
rewards could come from bridging the gap between synthetic molecular systems and the …
Abiotic chemical fuels for the operation of molecular machines
C Biagini, S Di Stefano - Angewandte Chemie, 2020 - Wiley Online Library
Natural molecular machines require a continuous fuel supply to perform motions and/or
remain in a functional state. Consequently, the aim of developing artificial devices and …
remain in a functional state. Consequently, the aim of developing artificial devices and …
Pyridyl-acyl hydrazone rotaxanes and molecular shuttles
We report on rotaxanes featuring a pyridyl-acyl hydrazone moiety on the axle as a
photo/thermal-switchable macrocycle binding site. The pyridyl-acyl E-hydrazone acts as a …
photo/thermal-switchable macrocycle binding site. The pyridyl-acyl E-hydrazone acts as a …
Bio-inspired molecular machines and their biological applications
MN Tasbas, E Sahin, S Erbas-Cakmak - Coordination Chemistry Reviews, 2021 - Elsevier
Molecular machines lie at the center of living systems by taking a role in all fundamental
processes that constitute life including cell division, cellular trafficking, and macromolecule …
processes that constitute life including cell division, cellular trafficking, and macromolecule …
Functional Rhythmic Chemical Systems Governed by pH‐Driven Kinetic Feedback
Hydrogen ion autocatalytic reactions, especially in combination with an appropriate negative
feedback process, show a wide range of dynamical phenomena, like clock behavior …
feedback process, show a wide range of dynamical phenomena, like clock behavior …
The synthesis of a rigid conjugated viologen and its cucurbituril pseudorotaxanes
Y Song, X Huang, H Hua, Q Wang - Dyes and pigments, 2017 - Elsevier
Abstract A linear viologen (bis [4-(4-pyridinyl) phenyl] viologen, BPPV) characterized by a
fully-conjugated structure was synthesized through Zinke reaction. BPPV consists of a …
fully-conjugated structure was synthesized through Zinke reaction. BPPV consists of a …
The Hydrolysis of the Anhydride of 2‐Cyano‐2‐phenylpropanoic Acid Triggers the Repeated Back and Forth Motions of an Acid–Base Operated Molecular Switch
C Biagini, G Capocasa, V Cataldi… - … A European Journal, 2019 - Wiley Online Library
This work aimed to render phenomenologically autonomous the otherwise stepwise
operation of a catenane‐based molecular switch, which is chemically triggered by the …
operation of a catenane‐based molecular switch, which is chemically triggered by the …
Multistimuli Sensitive Behavior of Novel Bodipy‐Involved Pillar [5] arene‐Based Fluorescent [2] Rotaxane and Its Supramolecular Gel
N Sun, X Xiao, W Li, J Jiang - Advanced Science, 2015 - Wiley Online Library
Fluorescent [2] rotaxane BC12P5 is successfully constructed with 1, 4‐diethoxypillar [5]
arene as wheel over a long alkyl axle with Bodipy chromophore as one stopper for the first …
arene as wheel over a long alkyl axle with Bodipy chromophore as one stopper for the first …