Diarylethenes spontaneously form the corresponding radical cations and carbocations upon inclusion within activated Ca Y zeolite; oxygen plays an important role in the generation of the radical cations
Cation radical Diels–Alder cycloadditions proceed via an acyclic intermediate that exists on a flat ...
By merging well-established concepts of supramolecular chemistry, protecting group strategy, and pho...
The yield of Norrish type I products are significantly enhanced when aryl alkyl ketones are photolyz...
Reactions of carbocations and radical cation of 1-phenyl 3,4-dihydronaphthalene have been investigat...
Radical cations of 1,1-diarylethylenes have been generated by direct excitation of the parent olefin...
Stable and ultrastable carbocations from 4-vinylanisole are spontaneously generated within zeolites;...
Zeolite is a porous highly interactive matrix. Zeolitic cations help to generate triplets from molec...
Inclusion of 1,1-diarylethylenes within activated CaY results in the formation of colored samples th...
Inclusion of 1,1-diarylethylenes within activated CaY results in the formation of colored samples th...
Inclusion of 4,4'-dimethylaminodiphenylethylene and related olefins within activated CaY results in ...
α-Alkyldibenzylketones included in cation exchanged faujasite type zeolites show photobehavior diffe...
The alkali ions present in the supercages of zeolites X and Y interact with included guest molecules...
Through a systematic study of several diphenylcyclopropane derivatives, we have inferred that the ca...
Carbocations are pervasive in contemporary organic synthesis, so new and innocuous methods of making...
Irradiation of 2-benzoyladamantane derivatives in zeolites yields the endo-cyclobutanols as the only...
Cation radical Diels–Alder cycloadditions proceed via an acyclic intermediate that exists on a flat ...
By merging well-established concepts of supramolecular chemistry, protecting group strategy, and pho...
The yield of Norrish type I products are significantly enhanced when aryl alkyl ketones are photolyz...
Reactions of carbocations and radical cation of 1-phenyl 3,4-dihydronaphthalene have been investigat...
Radical cations of 1,1-diarylethylenes have been generated by direct excitation of the parent olefin...
Stable and ultrastable carbocations from 4-vinylanisole are spontaneously generated within zeolites;...
Zeolite is a porous highly interactive matrix. Zeolitic cations help to generate triplets from molec...
Inclusion of 1,1-diarylethylenes within activated CaY results in the formation of colored samples th...
Inclusion of 1,1-diarylethylenes within activated CaY results in the formation of colored samples th...
Inclusion of 4,4'-dimethylaminodiphenylethylene and related olefins within activated CaY results in ...
α-Alkyldibenzylketones included in cation exchanged faujasite type zeolites show photobehavior diffe...
The alkali ions present in the supercages of zeolites X and Y interact with included guest molecules...
Through a systematic study of several diphenylcyclopropane derivatives, we have inferred that the ca...
Carbocations are pervasive in contemporary organic synthesis, so new and innocuous methods of making...
Irradiation of 2-benzoyladamantane derivatives in zeolites yields the endo-cyclobutanols as the only...
Cation radical Diels–Alder cycloadditions proceed via an acyclic intermediate that exists on a flat ...
By merging well-established concepts of supramolecular chemistry, protecting group strategy, and pho...
The yield of Norrish type I products are significantly enhanced when aryl alkyl ketones are photolyz...