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3‐Chloro‐3‐cyano‐1‐cyclohexyl‐4‐(phenylthio)‐2‐azetidinone. A substituted monocyclic β‐lactam

UC Irvine Previously Published Works (1980)

Creative Commons 'BY' version 4.0 license

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Peer Reviewed

(Hexafluoroacetylacetonato‐O,O')(1‐hydroxy‐2,2,6,6‐tetramethylpiperidinato‐O,N)palladium(II), [Pd(C5HF6O2)(C9H18NO)], a metal complex containing a reduced nitroxyl radical

UC Irvine Previously Published Works (1985)

Cover page: (Hexafluoroacetylacetonato‐O,O')(1‐hydroxy‐2,2,6,6‐tetramethylpiperidinato‐O,N)palladium(II), [Pd(C5HF6O2)(C9H18NO)], a metal complex containing a reduced nitroxyl radical

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Co‐crystallized bis(hexafluoroacetylacetonato)palladium(II) and 3‐cyano‐2,2,5,5‐tetramethyl‐2,5‐dihydropyrrolyl‐1‐oxyl, C10H2F12O4Pd.2C9H13N2O

UC Irvine Previously Published Works (1984)

Cover page: Co‐crystallized bis(hexafluoroacetylacetonato)palladium(II) and 3‐cyano‐2,2,5,5‐tetramethyl‐2,5‐dihydropyrrolyl‐1‐oxyl, C10H2F12O4Pd.2C9H13N2O

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3‐Bromo‐2,5‐diphenyl‐1,4‐dithiin 1,1‐dioxide

UC Irvine Previously Published Works (1980)

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Structure of (rac‐5,5,7,12,12,14‐hexamethyl‐1,4,8,11‐tetraazacyclotetradecane)silver(II) diperchlorate dihydrate

UC Irvine Previously Published Works (1993)

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Structure of (1,4,8,11‐tetramethyl‐1,4,8,11‐tetraazacyclotetradecane)silver(II) diperchlorate

UC Irvine Previously Published Works (1991)

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THE UTILITY OF ORGANOSAMARIUM(II) REAGENTS IN THE FORMATION OF POLYATOMIC GROUP-16 ELEMENT ANIONS

UC Irvine Previously Published Works (1994)

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Hydrogen‐bonding interactions in thiosemicarbazones of carboxylic acids: structure of 2‐ketobutyric acid thiosemicarbazone hemihydrate

UC Irvine Previously Published Works (1991)

Cover page: Hydrogen‐bonding interactions in thiosemicarbazones of carboxylic acids: structure of 2‐ketobutyric acid thiosemicarbazone hemihydrate

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Hydrothermal synthesis and characterization of mixed-valence hexatungstates: crystal structures of [(C2H5)(4)N](3)[(WW5O19)-W-V-O-VI]center dot 0.5H(2)O and [H3N(CH2)(2)NH3](2)[(WW5O19)-W-V-O-VI]center dot[H2N(CH2)(2)NH2]Cl center dot 8H(2)O

UC Irvine Previously Published Works (1998)

Cover page: Hydrothermal synthesis and characterization of mixed-valence hexatungstates: crystal structures of [(C2H5)(4)N](3)[(WW5O19)-W-V-O-VI]center dot 0.5H(2)O and [H3N(CH2)(2)NH3](2)[(WW5O19)-W-V-O-VI]center dot[H2N(CH2)(2)NH2]Cl center dot 8H(2)O

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Organo-functionalized metal–oxide clusters: synthesis and characterization of the reduced cationic species [NaV IV 6 O 6 {(OCH 2 CH 2 ) 2 NH} 6 ] +

UC Irvine Previously Published Works (2014)

A new heteropolyoxovanadium compound, [NaV6O6{(OCH2CH2)2NH}6]·(OH)0.5Cl0.5·3(H2O), was synthesized and characterized by single-crystal X-ray diffraction analysis, cyclic voltammetry, FTIR and UV-vis spectroscopy, and TGA. [NaV6O6{(OCH2CH2)2NH}6]·(OH)0.5Cl0.5·3(H2O) contains the diethanolamine functionalized oxovanadium cationic cluster, [NaV(IV)6O6{(OCH2CH2)2NH}6](+). The cluster cation is composed of a fully reduced cyclic {NaV6N6O18} framework which adopts an Anderson-like structure and is comprised of a ring of six edge-sharing {VO5N} octahedra linked to a central {NaO6} unit. Two (OCH2CH2-) arms of each of the six diethanolamine ligands are incorporated into the oxometalate core. FTIR spectra are consistent with the presence of expected V=Ot stretching modes and functionalization with diethanolamine. Electrochemical and UV-vis absorption properties are consistent with two distinct MLCT processes: the characteristic V=Ot dπ-pπ interaction, and a second process occurring through the hydrogen-terminated nitrogen atoms (V-N-H) of the octahedra forming the cyclic {NaV6N6O18} core.