2018
DOI: 10.1002/marc.201800142
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Recent Advances in Cyclodextrin‐Based Light‐Responsive Supramolecular Systems

Abstract: Cyclodextrins (CDs), one of the host molecules in supramolecular chemistry, can host guest molecules to form inclusion complexes via non-covalent and reversible host-guest interactions. CD-based light-responsive supramolecular systems are typically constructed using CDs and guest molecules with light-responsive moieties, including azobenzene, arylazopyrazole, o-nitrobenzyl ester, pyrenylmethyl ester, coumarin, and anthracene. To date, numerous efforts have been reported on the topic of CD-based light-responsiv… Show more

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Cited by 45 publications
(24 citation statements)
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“…[58] Thiol-ene "click" chemistry found widespread application in polymer chemistry and also made its way into the design of photoresponsive hydrogels. [66] Spiropyran isomerizes from the hydrophobic closering form to the hydrophilic open ring merocyanine zwitterion under the irradiation of 365 nm. [62,63] Notably, thiol or disulfide reactions proceeding via a radical mechanism are fundamen tally different from electrocyclic cycloadditions, which proceed via a concerted cyclic transition state.…”
Section: Molecular Mechanismsmentioning
confidence: 99%
“…[58] Thiol-ene "click" chemistry found widespread application in polymer chemistry and also made its way into the design of photoresponsive hydrogels. [66] Spiropyran isomerizes from the hydrophobic closering form to the hydrophilic open ring merocyanine zwitterion under the irradiation of 365 nm. [62,63] Notably, thiol or disulfide reactions proceeding via a radical mechanism are fundamen tally different from electrocyclic cycloadditions, which proceed via a concerted cyclic transition state.…”
Section: Molecular Mechanismsmentioning
confidence: 99%
“…In this context, the complexation of cyclodextrin (CD) hosts by azobenzene guests has been proven very valuable since the binding constants of E and Z isomers to the CD's hydrophobic cavity differ severely . Many supra‐ and macromolecular systems based on this azobenzene–CD interaction have been developed, in particular by Harada and co‐workers …”
Section: Photoswitching Bulk Materialsmentioning
confidence: 99%
“…In the past few decades, controllable supramolecular nanoassembly constructed by several kinds of weak noncovalent interactions [1,2] have attracted considerable research interest because of their ease of preparation and good practical application in functional materials and biochemistry. [3][4][5] Supramolecular assembly is an effective approach for the construction of nanoparticles that can effectively control the release of drugs at specific sites through external multi-stimulus, such as pH, [6,7] temperature, [8] light, [9,10] redox, [11,12] enzyme, [13] electricity. [2] Among the various stimuli, variation in pH is the most frequently used, as pH values in different tissues and cellular compartments vary tremendously.…”
Section: Introductionmentioning
confidence: 99%