Organometallic chalcogen complexes. XVII. Preparation and structural characterization of a metal-oxygen atom cluster system, Co3(.pi.-C5H5)3(CO)(O)

1969 ◽  
Vol 91 (14) ◽  
pp. 3763-3769 ◽  
Author(s):  
Vernon A. Uchtman ◽  
Lawrence F. Dahl
1969 ◽  
Vol 91 (6) ◽  
pp. 1574-1576 ◽  
Author(s):  
Robert G. Vranka ◽  
Lawrence F. Dahl ◽  
Paolo Chini ◽  
Joseph Chatt

1994 ◽  
Vol 47 (2) ◽  
pp. 359 ◽  
Author(s):  
JM Harrowfield ◽  
BW Skelton ◽  
AH White

The structural characterization of a new quasi- undecahydrate of samarium(III) picrate is described. [ Sm ( pic )2(OH2)6]( pic ).43/4H2O is monoclinic, C 2/c, a 39.96(1), b 7.951(2), c 24.233(9) Ǻ, β 110.92(2)°, Z = 8, temperature c.295 K; R was 0.047 for 5010 'observed' diffractometer reflections. Like the cations of Part I, the present has two picrate and six aqua ligands; although the general stereochemistry is similar, the picrate ligands are both clearly unidentate, unlike previous arrays wherein one behaves in a quasi- bidentate mode utilizing an ortho-nitro oxygen atom.


2021 ◽  
Vol 99 (2) ◽  
pp. 259-267
Author(s):  
Serge Ruccolo ◽  
Erika Amemiya ◽  
Daniel G. Shlian ◽  
Gerard Parkin

The silatrane hydride compound, [N(CH2CH2O)3]SiH, reacts with CO2 in the presence of the [tris(2-pyridylthio)methyl]zinc hydride complex, [Tptm]ZnH, to afford the silyl formate and methoxide derivatives, [N(CH2CH2O)3]SiO2CH and [N(CH2CH2O)3]SiOCH3. The molecular structure of [N(CH2CH2O)3]SiO2CH has been determined by X-ray diffraction, thereby demonstrating that the formate ligand adopts a distal conformation in which the uncoordinated oxygen atom resides with a trans-like disposition relative to silicon. Density functional theory calculations indicate that the atrane motif of [N(CH2CH2O)3]SiO2CH is flexible, such that the energy of the molecule changes relatively little as the Si···N distance varies over the range 2.0–3.0 Å.


2006 ◽  
Vol 61 (6) ◽  
pp. 753-757 ◽  
Author(s):  
Thorsten Glaser ◽  
Maik Heidemeier ◽  
Erich Krickemeyer ◽  
Hartmut Bögge

As part of our synthetic efforts for new triplesalen derivatives, we reacted 2,4,6-triacetyl- 1,3,5-trihydroxybenzene (1) with excess Cu(ClO4)2 · 6H2O, imidazole, and ethylenediamine. However, not the triple ketimine derivative was formed but the mononuclear CuII complex [LCuII(ImH)]ClO4 · 0.5EtOH · 0.5H2O (HL = 6-(1-(2-aminoethylimino)ethyl)-2,4-diacetyl-1,3,5-trihydroxybenzene) with only one ketimine function. This complex forms a one-dimensional coordination polymer in the solid state through the apical binding of a keto-oxygen atom of one cation to the CuII ion of a neighboring cation. Magnetic measurements reveal the presence of weak antiferromagnetic intra-chain interactions


1983 ◽  
Vol 249 (2) ◽  
pp. c35-c37 ◽  
Author(s):  
A. Ceriotti ◽  
L. Resconi ◽  
F. Demartin ◽  
G. Longoni ◽  
M. Manassero ◽  
...  

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