2015
DOI: 10.1016/j.jphotochemrev.2015.04.002
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Supramolecular photochemistry concepts highlighted with select examples

Abstract: ‗Supramolecular Photochemistry' (SP) deals with a study of the properties of molecules in their excited states where the medium plays a significant role. While ‗Molecular Photochemistry' (MP) deals with studies in isotropic solution, the SP deals with reactant molecules that interact weakly with their surroundings. The surroundings in general are highly organized assemblies such as crystals, liquid crystals, micelles, hostguest structures etc. The behavior of exited molecules in SP unlike in isotropic solution… Show more

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Cited by 58 publications
(36 citation statements)
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“…Photochemical reactions have significantly enriched the organic synthesis portfolio as it allows for the rapid construction of complex molecules using photons as a traceless reagent [6,7]. As a consequence, photochemical processes are currently becoming widespread [8], in particular in the search of new biologically active compounds for applications in medicine or agriculture, as well as in many other fields (healthcare, material and environmental sciences for instance) [9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…Photochemical reactions have significantly enriched the organic synthesis portfolio as it allows for the rapid construction of complex molecules using photons as a traceless reagent [6,7]. As a consequence, photochemical processes are currently becoming widespread [8], in particular in the search of new biologically active compounds for applications in medicine or agriculture, as well as in many other fields (healthcare, material and environmental sciences for instance) [9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…These 'nanoreactors' provide confined environments to induce selectivity, modulate the reaction pathway, and potentially catalyze the reaction [8]. Our group studies how the photolysis of small organic molecules is altered and influenced by the encapsulation within the cylindrical channels of stable, porous, crystalline hosts [9].…”
Section: Introductionmentioning
confidence: 99%
“…Since the first report in 1877 6 , UV light-induced [2 + 2] cycloaddition of alkenes has been conveniently used to generate cyclobutane backbones 7 . However, geometric isomerization and racemic background photoreactions facilely induced by UV light make the stereochemical control of cycloaddition a long-standing challenge, especially for acyclic alkenes 8,9 . As a green and clean procedure for chemical process and production that are contemporarily demanded by sustainable development, the visible-light sensitized intra-and intermolecular [2 + 2] cycloaddition of olefins has drawn great attention of chemical society in past decades [10][11][12][13][14][15] , leading to fast progress in [2 + 2] photocycloaddition of nonrigid olefins with excellent regio-and stereoselectivities [16][17][18][19][20] .…”
mentioning
confidence: 99%