1972
DOI: 10.1021/ic50109a037
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Crystal and molecular structure of di-2-(5-perfluoromethyltetrazolato)-.mu.-1,2-bis(diphenylphosphino)ethane-bis(1,2-bis(diphenylphosphino)ethane)dicopper(I),Cu2(CF3CN4)2((CH2P(C6H5)2)2)3

Abstract: Structure of Cu2 (CF3CN4)2 ((CH2P (CeH6) 2) 2);

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Cited by 61 publications
(17 citation statements)
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“…Evidence obtained to date indicates that either of the two isomers N(1) and N(2)-bonded are formed simultaneously [7,12,16,26,27] or only the N(2) bound isomer is produced exclusively [7,12,16,17]. In our cases both the N(1) and N(2) bonded isomers are formed depending on the substituents of the triazolato ring.…”
Section: Reaction Of Ruthenium Azido Complexes With Dmd or Dedmentioning
confidence: 46%
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“…Evidence obtained to date indicates that either of the two isomers N(1) and N(2)-bonded are formed simultaneously [7,12,16,26,27] or only the N(2) bound isomer is produced exclusively [7,12,16,17]. In our cases both the N(1) and N(2) bonded isomers are formed depending on the substituents of the triazolato ring.…”
Section: Reaction Of Ruthenium Azido Complexes With Dmd or Dedmentioning
confidence: 46%
“…In analogy, a coordinated azide group in metal complexes can also undergo such cycloaddition reactions [6]. Azido complexes undergo [3+2] cycloaddition reactions with nitriles [7][8][9][10][11][12][13][14][15][16][17][18][19] and isonitriles [7,8,[20][21][22][23] to produce tetrazolato complexes. Similar reactions with alkynes produce triazolates complexes [12,[24][25][26]; alkenes, however, react very slowly and mostly afforded mixture of products [8,12].…”
Section: Introductionmentioning
confidence: 99%
“…NMR spectra were recorded on an AMX-400 MHz spectrometer at 400. 13 ( 1 H), 161.97 ( 31 P) or 100.61 MHz ( 13 C) with SiMe 4 or 85% H 3 PO 4 as internal references and coupling constants are given in hertz. Infrared spectra were recorded as a KBr pellets on a Perkin-Elmer Model 983 spectrometer.…”
Section: Methodsmentioning
confidence: 99%
“…The 13 C{ 1 H} NMR spectra of these complexes exhibit multiplet signals at d 127.59-134.61 for the carbon of the phenyl group. 13 C { 1 H} NMR of the indenyl triazole complexes were also studied. Kohler [35b] proposed a correlation between 13 C{ 1 H} chemical shift of indenyl ring junction carbons, C(3a)-(7a) and hapacity of the coordinated ligand.…”
Section: 12mentioning
confidence: 99%
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