2004
DOI: 10.1016/j.poly.2003.08.021
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Erratum to: “Effect of free and chelating phosphine coordination environments on the NiS2P2 chromophore: synthesis, NMR and other spectral studies. Crystal and molecular structures of (N,N-dipropyldithiocarbamato)di(triphenylphosphine)nickel(II) perchlorate and (N,N-dipropyldithiocarbamato)1,2-bis((diphenylphosphino)ethane)nickel(II) tetraphenylborate” [Polyhedron 23 (2004) 77]

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Cited by 5 publications
(5 citation statements)
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“…In the compound [{Cu(etdtc)} 2 ppzdtc], a triplet was observed at 0.79 ppm for the methyl protons of diethyldithiocarbmato-groups, whereas the methylene protons were found to resonate at 3.73 ppm as multiplet. 28 Another singlet at 3.45 ppm was also observed corresponding to eight protons of the piperazine moiety, thus confirming the proposed structure of the compound (Scheme 2).…”
Section: H Nmrsupporting
confidence: 71%
“…In the compound [{Cu(etdtc)} 2 ppzdtc], a triplet was observed at 0.79 ppm for the methyl protons of diethyldithiocarbmato-groups, whereas the methylene protons were found to resonate at 3.73 ppm as multiplet. 28 Another singlet at 3.45 ppm was also observed corresponding to eight protons of the piperazine moiety, thus confirming the proposed structure of the compound (Scheme 2).…”
Section: H Nmrsupporting
confidence: 71%
“…The average bond length (Å) of C-S bond in these complexes is 1.72, which is significantly shorter than the C-S single bond length (1.81) and higher than the C=S distance (1.69). The observed intermediate value between the single bond (C-S) and the double bond (C=S) distances showed a partial double bond nature of the S¤C¤S bonds [15].…”
Section: Crystal Structuresmentioning
confidence: 92%
“…In these three complexes, the average length (Å) of C-S bond is 1.7138(4) which is significantly shorter than the CÀS single bond length (1.81) and higher than the C@S distance (1.69). The observed intermediate value between the CÀS and C@S bond distances indicated that a partial double bond nature arises due to the chelated sulfur atoms [18]. The powder XDR patterns of the complexes 6 and 9 (as representative cases) for which we are not able to prepare single crystals are also recorded to have an insight into the structure of the complexes.…”
Section: Crystal Structuresmentioning
confidence: 99%