Relative basicities of the oxygen atoms of the Linquist polyoxometalate [Mo6O19]2− and their recognition by hydroxyl groups in radical cation salts based on functionalized tetrathiafulvalene π donors

1999 ◽  
pp. 1241-1248 ◽  
Author(s):  
Anne Dolbecq ◽  
Aude Guirauden ◽  
Marc Fourmigué ◽  
Kamal Boubekeur ◽  
Patrick Batail ◽  
...  
Keyword(s):  
Radical Cation ◽  
Hydroxyl Groups ◽  
Radical Cation Salts ◽  
Oxygen Atoms

119Sn, 13C and 1H NMR Spectra of Tris(1-butyl)stannyl D-Glucuronate

1997 ◽  
Vol 62 (8) ◽  
pp. 1169-1176 ◽  
Author(s):  
Antonín Lyčka ◽  
Jaroslav Holeček ◽  
David Micák
Keyword(s):  
Chemical Shift ◽  
Carbonyl Group ◽  
1H Nmr ◽  
Equatorial Plane ◽  
Title Compound ◽  
Nmr Spectra ◽  
Hydroxyl Groups ◽  
Carboxylic Group ◽  
H Nmr ◽  
Oxygen Atoms

The 119Sn, 13C and 1H NMR spectra of tris(1-butyl)stannyl D-glucuronate have been measured in hexadeuteriodimethyl sulfoxide, tetradeuteriomethanol and deuteriochloroform. The chemical shift values have been assigned unambiguously with the help of H,H-COSY, TOCSY, H,C-COSY and 1H-13C HMQC-RELAY. From the analysis of parameters of 119Sn, 13C and 1H NMR spectra of the title compound and their comparison with the corresponding spectra of tris(1-butyl)stannyl acetate and other carboxylates it follows that in solutions of non-coordinating solvents (deuteriochloroform) the title compound is present in the form of more or less isolated individual molecules with pseudotetrahedral environment around the central tin atom and with monodentately bound carboxylic group. The interaction of tin atom with oxygen atoms of carbonyl group and hydroxyl groups of the saccharide residue - if they are present at all - are very weak. In solutions in coordinating solvents (hexadeuteriodimethyl sulfoxide or tetradeuteriomethanol), the title compound forms complexes with one molecule of the solvent. Particles of these complexes have a shape of trigonal bipyramid with the 1-butyl substituents in equatorial plane and the oxygen atoms of monodentate carboxylic group and coordinating solvent in axial positions.

scholarly journals New Radical Cation Salts Based on BDH-TTP Donor: Two Stable Molecular Metals with a Magnetic [ReF6]2− Anion and a Semiconductor with a [ReO4]− Anion

2021 ◽  
Vol 7 (4) ◽  
pp. 54
Author(s):  
Nataliya D. Kushch ◽  
Gennady V. Shilov ◽  
Lev I. Buravov ◽  
Eduard B. Yagubskii ◽  
Vladimir N. Zverev ◽  
...  
Keyword(s):  
Radical Cation ◽  
Low Temperatures ◽  
Ac Susceptibility ◽  
Slow Relaxation ◽  
Organic Radical ◽  
Inorganic Anion ◽  
Distinctive Features ◽  
Metallic Character ◽  
Radical Cation Salts ◽  
Partial Population

Three radical cation salts of BDH-TTP with the paramagnetic [ReF6]2− and diamagnetic [ReO4]− anions have been synthesized: κ-(BDH-TTP)4ReF6 (1), κ-(BDH-TTP)4ReF6·4.8H2O (2) and pseudo-κ″-(BDH-TTP)3(ReO4)2 (3). The crystal and band structures, as well as the conducting properties of the salts, have been studied. The structures of the three salts are layered and characterized by alternating κ-(1, 2) and κ″-(3) type organic radical cation layers with inorganic anion sheets. Similar to other κ-salts, the conducting layers in the crystals of 1 and 2 are formed by BDH-TTP dimers. The partial population of positions of Re atoms and disorder in the anionic layers of 1–3 are their distinctive features. Compounds 1 and 2 show the metallic character of conductivity down to low temperatures, while 3 is a semiconductor. The ac susceptibility of crystals 1 was investigated in order to test the possible slow relaxation of magnetization associated with the [ReF6]2− anion.

ChemInform Abstract: Tetrathiafulvalene-Based Radical Cation Salts with Transition Metal Bis(dicarbollide) Anions

ChemInform ◽  
2016 ◽  
Vol 47 (11) ◽  
pp. no-no
Author(s):  
Vladimir I. Bregadze ◽  
Oleg A. Dyachenko ◽  
Olga N. Kazheva ◽  
Andrey V. Kravchenko ◽  
Igor B. Sivaev ◽  
...  
Keyword(s):  
Transition Metal ◽  
Radical Cation ◽  
Radical Cation Salts

Molecular metals based on radical cation salts of ET and some its analogues with the photochromic nitroprusside anion, [Fe(CN)5NO]2−

1999 ◽  
Vol 102 (1-3) ◽  
pp. 1646-1649 ◽  
Author(s):  
L. Kushch ◽  
L. Buravov ◽  
V. Tkacheva ◽  
E. Yagubskii ◽  
L. Zorina ◽  
...  
Keyword(s):  
Radical Cation ◽  
Radical Cation Salts ◽  
Nitroprusside Anion

Substitutional and solvation effects on conformational equilibria. Effects on the interaction between opposing axial oxygen atoms

1969 ◽  
Vol 47 (23) ◽  
pp. 4441-4446 ◽  
Author(s):  
R. U. Lemieux ◽  
A. A. Pavia
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Hydrogen Bonding ◽  
Magnetic Resonance ◽  
Hydroxyl Groups ◽  
Evidence Based ◽  
Electrostatic Repulsion ◽  
Hydrogen Bridge ◽  
Conformational Equilibria ◽  
Free Hydroxyl ◽  
Oxygen Atoms

Evidence based both on nuclear magnetic resonance and rotation data primarily obtained from methyl 3-deoxy-β-L-erythro-pentopyranoside and a number of its derivatives is interpreted to show that the electrostatic repulsion between the oxygen atoms at the 2 and 4 positions is substantially less when these oxygens are linked to acyl groups than when in the form of either methyl ethers or as hydroxyl groups hydrogen bonded to solvent. Also, experimental evidence is presented which requires the hydrogen bridge between two axially disposed hydroxyl groups to be substantially strengthened by hydrogen bonding of the free hydroxyl by solvent.

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