Bis(arene)vanadium anions: a new class of organovanadium complexes. X-ray structural characterization of solvated K[(.eta.6-1,3,5-C6H3Me3)2V]

1988 ◽  
Vol 7 (2) ◽  
pp. 565-566 ◽  
Author(s):  
Giovanni. Fochi ◽  
Dario. Braga ◽  
Piera. Sabatino
1994 ◽  
Vol 219 (1-2) ◽  
pp. 7-10 ◽  
Author(s):  
F. Albert Cotton ◽  
Lee M. Daniels ◽  
Larry R. Falvello ◽  
Carlos A. Murillo

1995 ◽  
Vol 73 (7) ◽  
pp. 1044-1049 ◽  
Author(s):  
David E. Harwell ◽  
Juliet Nabakka ◽  
Carolyn B. Knobler ◽  
M. Frederick Hawthorne

The synthesis of bis-(1-carboranylmethyl) ether was first published in 1963; however, its subsequent complexation with a transition metal was never reported. We now report the complexation of cobalt and the corresponding X-ray structure for the triphenylmethylphosphonium salt of the cobalta-bis(carboranylmethyl) ether. The cobalt complex crystallized in the monoclinic space group C2/c with a = 21.729(6) Å, b = 9.845(2) Å, c = 35.565(9) Å, β = 105.363(9)°, V = 7336 Å3, and Z = 8. Data were collected using CuKα radiation, to a maximum 2θ = 115°, giving 4123 unique reflections, and the structure was solved by heavy atom methods. The final discrepancy index was R = 0.093, Rw = 0.100 for 1919 independent reflections with I > 3σ(I). This metala-bis(carboranylalkyl) ether is the first in a new class of Venus flytrap compounds (VFC), containing an ether linkage, to be synthesized as model compounds for the development of reagents suitable for use in the radioimmunodetection and radioimmunotherapy of cancer. Keywords: cobalt, radioimmunodetection, radioimmunotherapy, Venus flytrap.


2007 ◽  
Vol 2007 (suppl_26) ◽  
pp. 61-66 ◽  
Author(s):  
B. Peplinski ◽  
B. Adamczyk ◽  
G. Kley ◽  
K. Adam ◽  
F. Emmerling ◽  
...  

Author(s):  
Shabana Noor ◽  
Richard Goddard ◽  
Fehmeeda Khatoon ◽  
Sarvendra Kumar ◽  
Rüdiger W. Seidel

AbstractSynthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes with the formula [ZnLn(HL)(µ-OAc)(NO3)2(H2O)x(MeOH)1-x]NO3 · n H2O · n MeOH [Ln = Pr (1), Nd (2)] and the crystal and molecular structure of [ZnNd(HL)(µ-OAc)(NO3)2(H2O)] [ZnNd(HL)(OAc)(NO3)2(H2O)](NO3)2 · n H2O · n MeOH (3) are reported. The asymmetrical compartmental ligand (E)-2-(1-(2-((2-hydroxy-3-methoxybenzylidene)amino)-ethyl)imidazolidin-2-yl)-6-methoxyphenol (H2L) is formed from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation, resulting in a peripheral imidazoline ring. The structures of 1–3 were revealed by X-ray crystallography. The smaller ZnII ion occupies the inner N2O2 compartment of the ligand, whereas the larger and more oxophilic LnIII ions are found in the outer O2O2’ site. Graphic Abstract Synthesis and structural characterization of two heterodinuclear ZnII-LnIII complexes (Ln = Pr, Nd) bearing an asymmetrical compartmental ligand formed in situ from N1,N3-bis(3-methoxysalicylidene)diethylenetriamine (H2valdien) through intramolecular aminal formation are reported.


2012 ◽  
Vol 16 (01) ◽  
pp. 154-162 ◽  
Author(s):  
Edwin W.Y. Wong ◽  
Daniel B. Leznoff

The reduction of magnesium phthalocyanine (MgPc) with 2.2 equivalents of potassium graphite in 1,2-dimethoxyethane (DME) gives [K2(DME)4]PcMg(OH)(1) in 67% yield. Compound 1 was structurally characterized using single crystal X-ray crystallography and was found to be a monomeric, heterometallic complex consisting of a μ3-OH ligand that bridges a [MgIIPc3-]- anion to two potassium cations solvated by four DME molecules. An absorption spectrum of 1 confirms the Pc ligand is singly reduced and has a 3–charge. The solid-state structure of 1 does not indicate breaking of the aromaticity of the Pc ligand. Compound 1 is only the second Pc3- complex and the first reduced MgPc to be isolated and structurally characterized.


1997 ◽  
Vol 306 (2) ◽  
pp. 198-204 ◽  
Author(s):  
A.A. Darhuber ◽  
J. Stangl ◽  
V. Holy ◽  
G. Bauer ◽  
A. Krost ◽  
...  

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