Search results for "Radical"
showing 10 items of 1401 documents
CCDC 725617: Experimental Crystal Structure Determination
2009
Related Article: E.Coronado, C.Gimenez-Saiz, F.M.Romero, A.Tarazon|2009|Inorg.Chem.|48|2205|doi:10.1021/ic802218j
CCDC 191556: Experimental Crystal Structure Determination
2003
Related Article: I.Ratera, D.Ruiz-Molina, F.Renz, J.Ensling, K.Wurst, C.Rovira, P.Gutlich, J.Veciana|2003|J.Am.Chem.Soc.|125|1462|doi:10.1021/ja0282590
CCDC 1567091: Experimental Crystal Structure Determination
2020
Related Article: Amit Rajput, Anuj Kumar Sharma, Suman K. Barman, Francesc Lloret, Rabindranath Mukherjee|2018|Dalton Trans.|47|17086|doi:10.1039/C8DT03257B
Syntheses and Structures of Magnesium and Zinc Boraamidinates: EPR and DFT Investigations of Li, Mg, Zn, B, and In Complexes of the [PhB(NtBu)2]•- An…
2006
The first magnesium and zinc boraamidinate (bam) complexes have been synthesized via metathetical reactions between dilithio bams and Grignard reagents or MCl2 (M = Mg, Zn). The following new classes of bam complexes have been structurally characterized: heterobimetallic spirocycles {(L)μ-Li[PhB(μ-NtBu)2]}2M (6a,b, M = Mg, L = Et2O, THF; 6c, M = Zn, L = Et2O); bis(organomagnesium) complexes {[PhB(μ3-NtBu)2](MgtBu)2(μ3-Cl)Li(OEt2)3} (8) and {[PhB(μ3-NtBu)2](MgR)2(THF)2} (9a, R = iPr; 9b, R = Ph); mononuclear complex {[PhB(μ-NDipp)2]Mg(OEt2)2} (10). Oxidation of 6a or 6c with iodine produces persistent pink (16a, M = Mg) or purple (16b, M = Zn) neutral radicals {Lx-μ-Li[PhB(μ-NtBu)2]2M}• (L …
In Search of the [PhB(μ-NtBu)2]2As• Radical: Experimental and Computational Investigations of the Redox Chemistry of Group 15 Bis-boraamidinates
2008
DFT calculations for the group 15 radicals [PhB(μ-NtBu)2]2M• (M = P, As, Sb, Bi) predict a pnictogen-centered SOMO with smaller contributions to the unpaired spin density arising from the nitrogen and boron atoms. The reactions of Li2[PhB(μ-NR)2] (R = tBu, Dipp) with PCl3 afforded the unsolvated complex LiP[PhB(μ-NtBu)2]2 (1a) in low yield and ClP[PhB(μ-NDipp)2] (2), both of which were structurally characterized. Efforts to produce the arsenic-centered neutral radical, [PhB(μ-NtBu)2]2As•, via oxidation of LiAs[PhB(μ-NtBu)2]2 with one-half equivalent of SO2Cl2, yielded the Zwitterionic compound [PhB(μ-NtBu)2As(μ-NtBu)2B(Cl)Ph] (3) containing one four-coordinate boron center with a B−Cl bond.…
La experiencia del Mal Radical en la obra de Jorge Semprún = The experience of Radical Evil in the works of Jorge Semprún
2017
<p align="JUSTIFY"><span style="font-family: 'Book Antiqua', serif;"><span style="font-size: small;">Este artículo pretende realizar un análisis de las novelas sobre los campos de concentración del escritor Jorge Semprún. Partiendo de la dicotomía escribir o vivir como un estado psicológico del autor tras su liberación, se reflexionará sobre las posibilidades de la literatura y del artificio como transmisores capaces de hacer entender la experiencia concentracionaria. Finalmente, se analizará el concepto filosófico del Mal Radical, señalado por Semprún como un elemento clave para entender dicha experiencia.</span></span></p><p align="JUSTIFY"><sp…
Nitrogen-Doped Carbon Nanodots-Ionogels: Preparation, Characterization, and Radical Scavenging Activity
2018
Hybrid diimidazolium-based ionogels were obtained by dispersing nitrogen-doped carbon nanodots (NCNDs) in ionic liquid (IL) solutions and by using dicationic organic salts as gelators. The properties of the NCND-ionogels were studied in terms of thermal stability, mechanical strength, morphology, rheological, and microscopic analyses. Insights into the formation of the hybrid soft material were attained from kinetics of sol-gel phase transition and from estimating the size of the aggregates, obtained from opacity and resonance light-scattering measurements. We demonstrate that, on one hand, NCNDs were able to favor the gel formation both in the presence of gelating and nongelating ILs. On t…
Visible Light-Induced Sulfonylation/Arylation of Styrenes in a Double Radical Three-Component Photoredox Reaction
2019
Simultaneous sulfonylation/arylation of styrene derivatives is achieved in a photoredox-catalyzed three-component reaction using visible light. A broad variety of difunctionalized products is accessible in mostly excellent yields and high diastereoselectivity. The developed reaction is scalable and suitable for the modification of styrene-functionalized biomolecules. Mechanistic investigations suggest the transformation to be operating through a designed sequence of radical formation and radical combination.
Unveiling the nature of supramolecular crown ether–C60 interactions
2015
A series of exTTF-(crown ether)2 receptors, designed to host C60, has been prepared. The size of the crown ether and the nature of the heteroatoms have been systematically changed to fine tune the association constants, which were determined by a number of complementary spectroscopic techniques. Electrochemical measurements and transient absorption spectroscopy assisted in corroborating charge transfer in the ground state and in the excited state, leading to the formation of radical ion pairs featuring lifetimes in the range from 12 to 21 ps. To rationalize the nature of the exTTF-(crown ether)2$C60 stabilizing interactions, theoretical calculations have been carried out, suggesting a syner…
Nickel‐Mediated Photoreductive Cross Coupling of Carboxylic Acid Derivatives for Ketone Synthesis**
2021
A simple photochemical, nickel-catalyzed synthesis of ketones starting from carboxylic acids is presented. Hantzsch-ester (HE) functions as a cheap, green and strong photoreductant upon visible-light excitation to facilitate radical generation and also engages in the Ni-catalytic cycle to restore the reactive species. With this dual role, HE allows for the coupling of a large variety of radicals (1°,2°, benzylic, α-oxy & α-amino) with aroyl and alkanoyl moieties, a new feature in the synthesis of ketones through dual nickel photoredox catalysis. With both precursors deriving from abundant carboxylic acids, this protocol is a welcome addition to the organic chemistry toolbox. The reactio…