Coordination properties of the diethyl 2-pyridylmethylphosphonate ligand (2-pmpe) with chloride transition-metal salts: X-ray crystal structure of Cd4(2-pmpe)4Cl8

2007 ◽  
Vol 843 (1-3) ◽  
pp. 26-31 ◽  
Author(s):  
Bogumiła Żurowska ◽  
Jerzy Mroziński ◽  
Zbigniew Ciunik ◽  
Justyn Ochocki
Keyword(s):  
Crystal Structure ◽  
Transition Metal ◽  
Metal Salts ◽  
X Ray ◽  
Coordination Properties ◽  
Transition Metal Salts

Bis-2-thienyldiethylaminophosphane as a Ligand in Late Transition Metal Complexes and its Transformation to Bis-2-thienylphosphane

2014 ◽  
Vol 69 (11-12) ◽  
pp. 1429-1440
Author(s):  
Markus Granitzka ◽  
Peter Stollberg ◽  
Dietmar Stalke
Keyword(s):  
Nmr Spectroscopy ◽  
Transition Metal ◽  
Metal Complexes ◽  
Transition Metal Complexes ◽  
Metal Salts ◽  
Inert Gas ◽  
Late Transition Metal ◽  
X Ray ◽  
Transition Metal Salts ◽  
Late Transition

Abstract Bis-2-thienyldiethylaminophosphane (C4H3S)2PNEt2 (1) is introduced as a ligand for late transition metal complexes ([(H3C4S)2PNEt2]nMXmLp), with M = Ni(II), Au(I), Cu(I), Pd(II), Ir(I), X = Cl, Br and L = NCMe, COD, (2-7). Reactions of 1 with the late transition metal salts NiCl2·dme, (Me2S)AuCl, CuCl, PdCl2(PhCN)2, and [Ir(COD)Cl]2 yield the complexes [{(H3C4S)2PNEt2}2 · NiCl2] (2), [(H3C4S)2PNEt2 · AuCl] (3) [(H3C4S)2PNEt2·CuCl(CH3CN)]2 (4), [{(H3C4S)2PNEt2}2 · PdCl2] (5), [{(H3C4S)2PNEt2}2·PdCl2]2 (6), and [(H3C4S)2PNEt2·IrCl(COD)] (7). In addition, the transformation of 1 to the valuable chlorine-substituted starting material (H3C4S)2PCl (8) and the related conversion of 8 to the secondary phosphane (H3C4S)2PH (9) is reported. The complexes 2-7 are stable under inert gas conditions and were characterized by single-crystal X-ray studies, NMR spectroscopy, and elemental analysis.

X-Ray Absorption Edges of Transition Metal Salts

1956 ◽  
Vol 102 (3) ◽  
pp. 632-635 ◽  
Author(s):  
H. P. Hanson ◽  
J. R. Knight
Keyword(s):  
Transition Metal ◽  
Metal Salts ◽  
X Ray ◽  
Transition Metal Salts ◽  
X Ray Absorption ◽  
Absorption Edges

scholarly journals Synthesis of New Derivatives of BEDT-TTF: Installation of Alkyl, Ethynyl, and Metal-Binding Side Chains and Formation of Tris(BEDT-TTF) Systems

2021 ◽  
Vol 7 (8) ◽  
pp. 110
Author(s):  
Songjie Yang ◽  
Matteo Zecchini ◽  
Andrew Brooks ◽  
Sara Krivickas ◽  
Desiree Dalligos ◽  
...  
Keyword(s):  
Metal Binding ◽  
Tricarboxylic Acid ◽  
Metal Salts ◽  
Side Chain ◽  
Side Chains ◽  
Ethynyl Group ◽  
X Ray ◽  
Transition Metal Salts ◽  
Alkyl Side Chains ◽  
Derivatives Of

The syntheses of new BEDT-TTF derivatives are described. These comprise BEDT-TTF with one ethynyl group (HC≡C-), with two (n-heptyl) or four (n-butyl) alkyl side chains, with two trans acetal (-CH(OMe)2) groups, with two trans aminomethyl (-CH2NH2) groups, and with an iminodiacetate (-CH2N(CH2CO2−)2 side chain. Three transition metal salts have been prepared from the latter donor, and their magnetic properties are reported. Three tris-donor systems are reported bearing three BEDT-TTF derivatives with ester links to a core derived from benzene-1,3,5-tricarboxylic acid. The stereochemistry and molecular structure of the donors are discussed. X-ray crystal structures of two BEDT-TTF donors are reported: one with two CH(OMe)2 groups and with one a -CH2N(CH2CO2Me)2 side chain.

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