http://www.cnr.it/ontology/cnr/individuo/prodotto/ID192069
The Question of cis versus trans Configuration in Octahedral Metal Diketonates: An In-Depth Investigation on Diorganobis(4-acyl-5-pyrazolonato)- tin(IV) Complexes (Articolo in rivista)
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- The Question of cis versus trans Configuration in Octahedral Metal Diketonates: An In-Depth Investigation on Diorganobis(4-acyl-5-pyrazolonato)- tin(IV) Complexes (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1002/ejic.201101050 (literal)
- Alternative label
Francesco Caruso, Eric J. Chan, John V. Hanna, Fabio Marchetti,
Claudio Pettinari, Corrado Di Nicola, Riccardo Pettinari, Adriano Pizzabiocca,
Gregory J. Rees, David Quigley, Miriam Rossi, Brian W. Skelton,
Alexandre N. Sobolev, Allan H. White (2012)
The Question of cis versus trans Configuration in Octahedral Metal Diketonates: An In-Depth Investigation on Diorganobis(4-acyl-5-pyrazolonato)- tin(IV) Complexes
in European journal of inorganic chemistry (Print)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Francesco Caruso, Eric J. Chan, John V. Hanna, Fabio Marchetti,
Claudio Pettinari, Corrado Di Nicola, Riccardo Pettinari, Adriano Pizzabiocca,
Gregory J. Rees, David Quigley, Miriam Rossi, Brian W. Skelton,
Alexandre N. Sobolev, Allan H. White (literal)
- Pagina inizio
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://onlinelibrary.wiley.com/doi/10.1002/ejic.201101050/abstract (literal)
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroFascicolo
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Chimica Biomolecolare, Consiglio Nazionale delle
Ricerche, c/o Università di Roma \"La Sapienza\",
Piazzale Aldo Moro, 5, 00185 Roma, Italy; Chemistry M313, School of Biomedical, Biomolecular and
Chemical Sciences, The University of Western Australia,
Crawley, WA 6009, Australia; Department of Physics, University of Warwick,
Gibbet Hill Rd., Coventry CV4 7AL, UK; School of Science and Technology, Università degli Studi di
Camerino, Camerino (MA), Italy; Vassar College, Department of Chemistry,
Poughkeepsie, New York 12604-0484, USA (literal)
- Titolo
- The Question of cis versus trans Configuration in Octahedral Metal Diketonates: An In-Depth Investigation on Diorganobis(4-acyl-5-pyrazolonato)- tin(IV) Complexes (literal)
- Abstract
- Diorganotin(IV) derivatives of 4-acyl-5-pyrazolones Q2SnR2 [HQ = 3-methyl-1-phenyl-4-R-5-pyrazolone: HQnPe, R = neopentylcarbonyl; HQiPr, R = isopropylcarbonyl; HQtBu, R = tert-butylcarbonyl; HQCy, R = cyclohexylcarbonyl; HQCp, R = cyclopentylcarbonyl; HQEtCp, R = (ethylcyclopentyl)carbonyl] have been synthesized and characterized spectroscopically (IR, far-IR, 1H, 13C and 119Sn NMR) and structurally (X-ray). Steric bulkiness in the acyl fragment of HQtBu induces partial dissociation in solution of (QtBu)2SnMe2, which exists as an equilibrium mixture of six- and five-coordinate tin species. Single-crystal X-ray structure determinations of several representative complexes are presented. Whereas the dialkyltin(IV) complexes are always trans-octahedral, a diphenyltin(IV) derivative exists in the solid state that has the two phenyl groups in a cis arrangement. DMol3 and CASTEP DFT studies of this unprecedented cis, and the corresponding trans configurations, show the former to be slightly more stable, in agreement with the diffraction study. Solid-state 119Sn cross-polarization magic-angle spinning NMR spectroscopic data show that the isotropic chemical shifts (?iso,mas) and chemical-shift anisotropies/spans (??/?) that characterize the diphenyl(IV) derivatives are markedly removed from values measured for the corresponding dimethyl and di-n-butyl derivatives, thereby adding further evidence for a stable cis configuration in the diphenyl(IV) systems. This is supported by GIPAW DFT calculation of the 119Sn isotropic shifts and chemical-shift anisotropies/spans from fully relaxed structures by using the CASTEP code, which provides a direct link between the cis diphenyl(IV) arrangement and the reported differences in the 119Sn NMR spectroscopic parameters. (literal)
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