Ruthenium complexes with ferrocene-based P,C,P pincer ligand

First ruthenium complexes with a ferrocene-based pincer ligand were synthesized. The cyclometallation of 1,3-bis[(di-tert-butylphosphino)methyl]ferrocene with RuCl₂(DMSO)₄ in 2-methoxyethanol afforded the RuCl(CO)[{2,5-(Bu^t ₂PCH₂)₂C₅H₂}Fe(C₅H₅)](RuCl(CO) ) complex (5). Complex 5 reversibly binds CO to form the RuCl(CO)₂ complex (6). The analogous reaction in the presence of NaBAr′₄ (Ar′ = 3,5-(CF₃)₂C₆H₃) produced the cationic complex {Ru(CO)₂ }BAr′₄ (7). The structures of complexes 5 and 7 were established by single-crystal X-ray diffraction. The X-ray diffraction study revealed an agostic interaction between one of the C-H bonds of the axial (exo-oriented with respect to the ferrocene iron atom) tert-butyl group and the Ru atom in complexes 5 and 7. Dedicated to Academician G. A. Abakumov on the occasion of his 70th birthday. Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 9, pp. 1695–1701, September, 2007.     

Comparative study of NMR spectea of monosubstituted (C5H4X)M(CO)3 (M=Mn,Re)

Conclusions The electron density on the-cyclopentadienyl ligand in cyclopentadienylmanganese tricarbonyl derivatives is higher than in the corresponding cyclopentadienylrhenium tricarbonyl derivatives.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 9, pp. 2142–2143, September, 1973.     

Alkylation of Phosphorylmethylenetriphenylphosphoranes

Abstract

Direction of alkylation of phosphoranes (I) depends on the nature of the substituent Y and the alkylating agent. Unsubstituted phosphorane reacts with CH₃J yielding only the product of C-methylation (II), whereas the reaction with Me₂SO₄ proceeds at both ends of the OPC-triad, preferably yielding the O-alkylation product (IIIa, 80%).     

A novel approach to the synthesis of amino acids based on cobalt bis(dicarbollide)

A novel approach to the synthesis of boron-containing amino acids based on ring opening of cyclic oxonium derivatives of polyhedral boron hydrides under the action of the terminal functional groups of natural amino acids was proposed. This approach was successfully implemented for the synthesis of cobalt bis(dicarbollide) — tyrosine conjugate.     

Reinvestigation of the Nazarov cyclization of 1-(3-hydroxypropynyl)cyclododecan-1-ol to bicyclo[10.3.0]pentadec-1(12)-en-13-one

Reinvestigation of the acid-catalyzed cyclization of 1-(3-hydroxypropynyl)cyclododecan-1-ol under the conditions of the Nazarov reaction demonstrated that this conversion yields two isomeric bicyclic ketones, namely, bicyclo[10.3.0]pentadec-1(12)-en-13-one and bicyclo[10.3.0]pentadec-1-en-3-one. The latter compound is thermodynamically less stable. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 7, pp. 1325–1327, July, 1997.     

Atropisomerism of phosphorus-containing N-aryl carbamates. Experimental and computational data

Studies by ¹H NMR spectroscopy and X-ray diffraction analysis revealed hindered rotation of the aromatic substituent about the C_Ar—N bond in ortho-substituted (except for o-fluorine-substituted) phosphorus-containing carbamates. The energy barriers to rotation (G _c ) and coalescence temperatures (T _c) determined by the coalescence method increase with increasing volume of the ortho substituent. Conformations resulting from rotation of the ortho-substituted aryl group about the C_Ar—N bond were analyzed by quantum-chemical methods, potential curves were constructed, and differences between the conformational energies and the heights of rotation barriers were estimated. The theoretical rotation barriers change in parallel with the experimental values of G _c ; however, the theoretical values are much smaller in magnitude.