Results 241 to 250 of about 35,108 (280)
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A Carbene−Carbene Complex Equilibrium
Journal of the American Chemical Society, 2010Phenylchlorocarbene, generated by laser flash photolysis of phenylchlorodiazirine, formed highly stable pi-type complexes with 1,3,5-trimethoxybenzene in pentane. The carbene and carbene complexes were in equilibrium. We measured the equilibrium constant (K = 1264 M(-1) at 294 K) and, from its temperature dependence, extracted the associated ...
Christina M. Odorisio+3 more
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Ultrafast Carbene−Carbene Isomerization
Journal of the American Chemical Society, 2008The photochemistry of two isomeric aryl diazo ketones was investigated by fs time-resolved UV-vis and IR spectroscopies. Both diazo ketone excited states decompose in less than 300 fs by multiple pathways. One pathway involves concerted Wolff rearrangement and nitrogen extrusion, most likely in the syn rotomer. In the anti rotomer of one isomer, oxygen
Gotard Burdzinski+4 more
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Bond Dissociation Energies of Carbene–Carbene and Carbene–Main Group Adducts
The Journal of Physical Chemistry A, 2022A range of carbene structures and their adducts with one another and with a selection of small-molecule electrophiles and nucleophiles were examined at the composite correlated molecular orbital theory G3MP2 level to explore ground-state "carbenic" structures, their stabilities, and reactivities.
Monica Vasiliu+7 more
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ChemInform Abstract: Carbenes and Nitrenes
ChemInform, 2004AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
David M. Hodgson+2 more
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Are There Carbenes in N‐Heterocyclic Carbene Organocatalysis?
Angewandte Chemie International Edition, 2017AbstractAzolium cations are widely employed in organocatalysis to catalyse highly valuable synthetic processes in the presence of a base. These reactions are called “N‐heterocyclic carbene catalysis”, based on the assumption that they are initiated by the formation of a free carbene through deprotonation, which can then react with the substrates and ...
Oldamur Hollóczki+2 more
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ChemInform Abstract: CARBEN‐CARBEN‐UMLAGERUNGEN
Chemischer Informationsdienst, 1973AbstractBei Temperaturen zwischen 250 und 600°C wird Phenylcarben (Ia) in das Carben (IIa) umgelagert, das zum Heptafulvalen (IIIa) dimerisiert.
T L Davis+7 more
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ChemInform, 1997
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
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AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
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ChemInform Abstract: Carbenes and Nitrenes
ChemInform, 1989AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.
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Formation of a pyrrole by carbene - carbene rearrangement
Tetrahedron Letters, 1982Abstract A pyrrole is formed through a carbene-carbene rearrangement, as shown by specific 12 C labelling experiments.
Lars Skattebøl, Jacek Arct
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