Preparation and crystallographic characterization of Pd(II) complexes containing imidobis(diphenylthiophosphinato) ligand

WOS: 000249905900011The reactions of PdCl2(L-L) [L-L = Ph2PCH2PPh2(dppm), Ph2PCH2CH2PPh2(dppe) and Ph2PCH2CH2CH2PPh2(dppp)] with equivalent amount of (Ph2P(S)NHP(S)Ph-2)(dppaS(2)) gave the complexes [Pd(L-L)(dppaS(2)-H)]ClO4 [L-L = dppm (1), dppe (2), dppp (3)]. The different synthetic route was used for complex 2 by using of Pd(dppe)Cl-2 and K[N(PSPh2)(2)] as starting materials (2a). All of these complexes have been characterized P-31{H-1} NMR, IR and elemental analyses. The complexes 2, 2a and 3 were crystallographically characterized. The coordination geometry around the Pd atoms in these complexes distorted square planar. Six membered dppaS2-H rings are twist boat conformations in three complexes. (C) 2007 Elsevier Ltd. All rights reserved

Poly[[diaquacaesium(I)]bis(mu(3)-3-carboxy-pyrazine-2-carboxylato)]

WOS: 000248149900019The asymmetric unit of the title compound, [Cs(C6H3N2O4)(2)(H2O)(2)](n), contains one Cs-I cation on an inversion centre, one 3-carboxypyrazine-2-carboxylate anion and one water molecule. In the crystal structure, each anion is linked to three cations, while each cation is surrounded by six of the anions. In addition, each cation is coordinated by two water O atoms, raising the coordination number to ten. In the crystal structure, intermolecular O - H center dot center dot center dot O and O - H center dot center dot center dot N hydrogen bonds contribute to the stabilization of the structure

Coupling of cyclopropylcarbene-chromium complex with ferrocenyl alkynes: synthesis of 5-ferrocenyl-5-hydroxy-2-cyclopentenones and 4-ferrocenyl-4-cyclopentene-1,3-diones

The coupling of ferrocenyl alkynes with cyclopropylcarbene-chromium complex leads to ferrocenyl-substituted 2-cyclopentenones with or without a hydroxy substituent, namely 4-cyclopentene-1,3-diones, 2-cyclobutenones, and alpha, beta-unsaturated aldehydes in varying amounts. The reaction initially produces a cyclopentadienone intermediate, then to the double bond of which, bearing a ferrocenyl group, addition of water occurs to afford hydroxy-substituted 2-cyclopentenones. In all the products, the hydroxy group ends up oc to the ferrocenyl moiety. In contrast, where no addition of water occurs, the alkenic bond is reduced to give 2-cyclopentenones. A secondary reaction product, namely 4-cyclopentene-1,3-dione, is formed by hydrolysis of the cyclopentadienome intermediates

2-(6-Oxo-3,4-diphenyl-1,6-dihydropyridazin-1-yl)acetic acid

In the title compound, C18H14N2O3, the pyridazine ring makes dihedral angles of 72.73 (11) and 49.97 (10)degrees with the two phenyl rings. The dihedral angle between the two phenyl rings is 52.42 (12)degrees. The crystal structure is stabilized by intermolecular O-H center dot center dot center dot O and C-H center dot center dot center dot O hydrogen-bonding interactions

Coupling of pentacarbonyl[(cyclopropyl)methoxymethylene]molybdenum complex with ferrocenylalkynes: Synthesis of ferrocenyl-substituted cycloheptadienones and cycloheptenediones

Pentacarbonyl[(cyclopropyl)methoxymethylene ]molybdenum complex reacts with ferrocenyl alkynes to afford ferrocenyl-substituted 2,4-cycloheptadienones as major products, accompanied by varying amounts of 2-cycloheptene-1,4-diones and/or 2-cyclobutenones. 2-Cycloheptene-1,4-diones are secondary reaction products and result from initially formed 2,4-cycloheptadienones via hydrolysis. In one reaction, a hydroxy-substituted 2,4-cycloheptadienone derivative was isolated, which was not observed previously from similar reactions

Efficient synthesis of some oxalacetic acid and pyruvic acid derivatives from the reactions of 2,3-furandiones with 2-phenylindole

Oxalacetic acid and pyruvic acid derivatives have been synthesized efficiently in high yields by the treatment of 4-ethoxycarbonyl-5phenyl-2,3-furandione and 4-benzoyl-5-phenyl-2,3-furandione with 2-phenylindole at room temperature and converted to simple derivatives such as an ester or a hydrazone. (C) 2008 Elsevier Ltd. All rights reserved

Synthesis of ferrocenyl pyrazoles by the reaction of 3-ferrocenylpropynal with hydrazinium salts

Synthesis of ferrocenyl-substituted pyrazoles via the reaction between 3-ferrocenylpropynal and hydrazinium salts is described. Depending upon the substitution pattern of hydrazine derivative, the reaction affords 1-alkyl/aryl-5-ferrocenylpyrazoles and/or 1-alkyl/aryl-3-ferrocenylpyrazoles. Structures of 5-ferrocenyl-1-phenyl-1H-pyrazole, 1-benzyl-5-ferrocenyl-1H-pyrazole and 2-(3-ferrocenylpyrazol-1-yl)ethanol were identified by X-ray crystallography

Synthesis and crystal structure of square-planar and mixed ligand octahedral nickel(II) O,O '-dicyclopentyl dithiophosphate complexes

TAS, MURAT/0000-0002-2879-6501WOS: 000252610900005Ammonium O,O'-dicyclopentylphosphorodithioate (dcpdtp) has been synthesized from phosphorus pentasulphide and cyclopentanol in the presence of ammonia gas. Its complexes, I=[Ni(dcpdtp)(2)] and II= [Ni(bP)(2)(dcpdtp)(2)] (bp=4-benzylpiperidine), have been synthesized and their structures characterized by using UV-vis, IR spectroscopy, magnetic susceptibility measurements and X-ray single crystal structural analysis. The complexes crystallize in the triclinic system (space groups P (1) over tilde) and exhibit a slightly distorted square planar [NiS4] and trans-octahedral [NiS4N2] geometry for the complexes I and II, respectively