Crystal and molecular structure of the charge-transfer salt of decamethylferrocenium and tricyanomethanide, [Fe(C5Me5)2]+/[C(CN)3]-. The electronic structure and spectra of the tricyanomethanide ion

1986 ◽  
Vol 108 (10) ◽  
pp. 2582-2588 ◽  
Author(s):  
David A. Dixon ◽  
Joseph C. Calabrese ◽  
Joel S. Miller
Keyword(s):  
Molecular Structure ◽  
Electronic Structure ◽  
Charge Transfer ◽  
Crystal And Molecular Structure

Synthese und Molekülgeometrie von Dichloro[η2-bis(di-r-butylphosphino)methan]pIatin(II), Pt(dtbpm)Cl2. Die Elektronenstruktur von 1,3-Diphosphaplatinacyclobutan-Fragmenten / Synthesis and Molecular Structure of Dichloro[η2-bis(di-t-butylphosphino)methane]platinum(II), Pt(dtbpm)Cl2. The Electronic Structure of 1,3-Diphosphaplatinacyclobutane Fragments

1987 ◽  
Vol 42 (4) ◽  
pp. 395-409 ◽  
Author(s):  
Peter Hofmann ◽  
Helmut Heiß ◽  
Gerhard Müller
Keyword(s):  
Molecular Structure ◽  
Electronic Structure ◽  
Crystal And Molecular Structure ◽  
Cone Angle ◽  
Membered Ring ◽  
Experimental Investigations ◽  
Molecular Orbital Calculations ◽  
X Ray Diffraction ◽  
X Ray ◽  
Potential Precursor

Based upon the experimentally known but yet unexplained very different reactivities of the two isoelectronic and isolobal intermediates Pt(PMe3)2 and Pt(PEt3)2, the electronic structure and bonding capability of such 14 electron fragments as a function of their geometry (P-Pt-P angle α, determined by the phosphane cone angle) are investigated using molecular orbital calculations. A decrease of the P-Pt -P angle leads to an exceptionally pronounced energy ascent of the b2-HOMO of Pt(PR3)2 species, which, as a consequence, might lead to unusual reactivity patterns and bonding capabilities of 1,3-diphosphaplatinacyclobutane fragments, for which an extreme electronic situation is enforced by steric constraints. Dichloro[η2-bis(di-r-butylphosphino) methane]platinum(II), Pt(dtbpm)Cl2, is synthesized as a potential precursor of Pt(dtbpm), in order to allow experimental investigations of this taylor made four-membered ring chelate complex of Pt(0). The crystal and molecular structure of Pt(dtbpm)Cl2 · 2 CHCl3 has been determined by X-ray diffraction.

The Crystal and Molecular Structure of Charge-Transfer Complex of Azo Dyestuff 5-(4-Chloro-2-nitrophenyl)-azo-6-hydroxy-1-ethyl-3-cyano-4-methyl-2-pyridone with Naphthalene

1993 ◽  
Vol 58 (9) ◽  
pp. 2121-2127 ◽  
Author(s):  
Josef Přikryl ◽  
Bohumil Kratochvíl ◽  
Jan Ondráček ◽  
Jaroslav Maixner ◽  
Jiří Klicnar ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Charge Transfer ◽  
Pyridine Ring ◽  
Charge Transfer Complex ◽  
Crystal And Molecular Structure ◽  
Crystal Packing ◽  
Direct Methods ◽  
Van Der Waals Forces ◽  
Triclinic Space Group ◽  
Π Stacking Interaction

The title charge-transfer complex crystallizes in the ratio of two molecules of azo dyestuff to one molecule of naphthalene. The crystals are triclinic, space group P1, lattice parameters a = 7.953(1), b = 11.608(2), c = 11.717(2) Å, α = 101.89(2), β = 94.27(2), γ = 109.91(2)°, Z = 2. The structure was solved by direct methods and refined anisotropically to R = 0.054 for 1 768 unique observed reflections. Crystal packing is stabilized by van der Waals forces and partly by π-π stacking interaction among naphthalene, phenyl and pyridine ring of pyridon azo dyestuff.

Interaction of diiodine with some tetra-substituted dithiooxamides. Crystal and molecular structure of bis(morpholinothiocarbonyl)bis(diiodine)

1988 ◽  
Vol 66 (6) ◽  
pp. 1483-1489 ◽  
Author(s):  
Davide Atzei ◽  
Paola Deplano ◽  
Emanuele F. Trogu ◽  
Francesco Bigoli ◽  
Maria Angela Pellinghelli ◽  
...  
Keyword(s):  
Molecular Structure ◽  
Charge Transfer ◽  
Solid State ◽  
Torsion Angle ◽  
Crystal And Molecular Structure ◽  
Formation Constants ◽  
Dalton Trans ◽  
X Ray ◽  
Space Groups ◽  
Spectrophotometric Methods

The reaction of some tetra-substituted dithiooxamides R2NC(S)C(S)NR2 (R = CH3:Me4dto; R = C2H5:Et4dto; R2N = OC4H8N:Mo2dto) with diiodine has been investigated by spectrophotometric methods in CHCl3. The formation in solution of 1:1 and 1:2 charge-transfer (c.t.) complexes between the reagents has been observed. A new computer program, derived from "SUPERQUAD" (P. Gans, A. Sabatini, and A. Vacca. J. Chem. Soc. Dalton Trans. 1195 (1985)), has been applied to evaluate the formation constants. The 1:2 c.t. complexes have been isolated in the solid state, and an X-ray structure analysis of the [OC4H8NC(S)C(S)NC4H8O]•2I2 compound indicated that the crystals are triclinic, space groups [Formula: see text], with a = 14.659(6), b = 15.111(6), c = 9.317(5) Å, α = 92.29(2), β = 99.71(2), γ = 99.48(2)° and Z = 4. In particular the torsion angle S—C—C—S (≈90°) shows that the conformation of the dithiooxamide is not trans.

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