The bimolecular quenching rate constants of singlet oxygen ((1)O2) by cubane and cubane derivatives were determined and found to be in the order of 10(3)-10(4) M(-1) s(-1). These values represent larger values than expected for aliphatic alkanes as a model for C-H vibrational deactivation. This result is explained by the occurrence of two different deactivation mechanisms: energy transfer to cubane C-H vibrational modes and the formation of a charge-transfer complex between (1)O2 and cubane ((1)O2(*-)...cubane(*+)).
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http://dx.doi.org/10.1021/ol802113j | DOI Listing |
Adv Sci (Weinh)
January 2024
CAS Key Laboratory of Materials for Energy Conversion, Department of Materials Science and Engineering, University of Science and Technology of China, Hefei, Anhui, 230026, China.
With the CoO slabs consisting of Co O cubane structure, layered Na CoO are considered promising candidates for oxygen evolution reaction (OER) in alkaline media given their earth-abundant and structural advantages. However, due to the strong adsorption of intermediates on the large basal planes, Na CoO cannot meet the activity demands. Here, a novel one-pot synthesis strategy is proposed to realize the high solubility of iron in Na CoO in an air atmosphere.
View Article and Find Full Text PDFDalton Trans
January 2014
Laboratoire de Chimie de Coordination, UMR 7177 CNRS/Université de Strasbourg, Institut Le Bel, 4, Rue Blaise Pascal, CS90032, 67081 Strasbourg Cedex, France.
The reaction of one equivalent of 2-methyl-1-(pyridin-2-yl)propan-2-ol (HL) with two equivalents of [Ni(OAc)2·4H2O] in methanol afforded the nonanuclear coordination cluster [Ni9(HL-κ(2)N,O)4(OAc-κ(2)O)2(μ2-OAc-κ(1)O)2(μ2-OAc-κ(2)O,O')4(μ3-OAc-κ(2)O;κ(2)O,O')2(μ3-OMe)8] (1). All nickel ions are hexacoordinated and show a slightly distorted octahedral coordination geometry. This unusual centrosymmetric coordination cluster can be described as constituted by two cubane moieties connected by a linker comprising a nickel atom, situated on the inversion centre, four bridging acetates and two triply-bridging acetates.
View Article and Find Full Text PDFOrg Lett
December 2008
Department of Chemistry, Columbia University, New York, New York 10027, USA.
The bimolecular quenching rate constants of singlet oxygen ((1)O2) by cubane and cubane derivatives were determined and found to be in the order of 10(3)-10(4) M(-1) s(-1). These values represent larger values than expected for aliphatic alkanes as a model for C-H vibrational deactivation. This result is explained by the occurrence of two different deactivation mechanisms: energy transfer to cubane C-H vibrational modes and the formation of a charge-transfer complex between (1)O2 and cubane ((1)O2(*-).
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