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Dihydrobis borate

Complexes of the titanium and vanadium groups are searee but mainly follow the routine eoordination modes. Sometimes for the dihydrobis(pyrazol-l-yl) borates, the role of M - - - H—B agostie interaetions is signifieant. [Pg.226]

From dihydrobis(l-imidazolyl)borate or tetrakis(l-imidazolyl)borate and silver salts the interesting mixed tetrametallic macrocycles 24 and 25 (Fig. 8) are prepared in high yields (40-60%) [36]. [Pg.10]

Bardwell, D. A. Jeffery, J. C. Jones, P. L. McCleverty, J. A. Psillakis, E. Reeves, Z. R. Ward, M. D. Lanthanide complexes of the tetradentate N-donor ligand dihydrobis[3-(2-pyridyl)pyrazolyl]borate and the terdentate N-donor ligand 2,6-bis(lH-pyrazol-3-yl)pyridine syntheses, crystal structures and solution structures based on luminescence lifetime studies. J. Chem. Soc., Dalton Trans. 1997, 2079-2086. [Pg.423]

Potassium dihydrobis(l-pyrazolyl)borate, m.p. 171-172°C., is a white crystalline solid, highly soluble in water and polar solvents. It may be recrystallized from anisole, but with large solubility losses. The infrared spectrum has a complicated BH2 stretch multiplet in the 2200-2500-cm.-1 range. It is very soluble in water and alcohols, but the ligand undergoes slow solvolysis, and solutions should be made up just before use. [Pg.101]

D. BIS[DIHYDROBIS(l-PYRAZOLYL)BORATO]NICKEL(II)— TRANSITION-METAL POLY (l-PYRAZOLYL)BORATES... [Pg.104]

Potassium dihydrobis(l-pyrazolyl)borate (18.6 g., 0.1 mole) of the solid as prepared in Sec. A is stirred in 300 ml. of distilled water, and any insolubles are removed by filtration. To the resulting clear solution is added, with stirring, 100 ml. of 0.5 M solution of nickel(II) acetate [or any other Ni(II) salt]. A yellowish precipitate forms immediately. The mixture is stirred at room temperature for 10 minutes and is then filtered. The solid is washed with copious amounts of water, then with... [Pg.104]

Pyrazaboles substituted on either the ring or the boron may be obtained by reaction between the appropriately substituted pyrazole and the appropriately substituted borane.11 For example the 2,6-dibromo-4,4,8,8-tetraethylpyrazabole can be made by the reaction between 4-bromopyrazole and pyrophoric triethylborane in xylene at reflux temperature. Another route to such compounds involves the dihydrobis(l-pyrazolyl)borate... [Pg.108]

Dihydrobis (pyrazolyl )borate Dihydrobis (3,5-dim ethylpy razolyl )borate Cholecystokinin Cyclohexanedionedioxime Central nervous system 2-(Diphenylphosphanyl)benzoic acid 2,3-Diaminopropionic acid Electrospray ionization mass spectrometry Fourier transform IR Gastrin-releasing peptide... [Pg.46]

X-ray crystal structure of the potassium dihydrobis(3-nitro-l,2,4-triazolyl) borate is reported [170], The potassium salt is polymeric and shows several K...N and K...0 interactions. [Pg.176]

Lanthanide complexes with dihydrobis(benzimidazolyl)borate for which a seven-coordinate polymeric structure was proposed have been described by Khan and co-workers.171... [Pg.188]

The ligand dihydrobis(3,4,5-tribromopyrazol-l-yl)borate, (BpBr3), and its derivative [Mo(BpBr3)(t 3-methallyl)(CO)2] have been prepared and characterized by Trofimenko and coworkers who compared the structure of the Mo complex with that of [Mo(Bp )(t 3-methallyl) (C O) 2 ].152... [Pg.29]


See other pages where Dihydrobis borate is mentioned: [Pg.168]    [Pg.169]    [Pg.192]    [Pg.197]    [Pg.199]    [Pg.203]    [Pg.218]    [Pg.221]    [Pg.221]    [Pg.225]    [Pg.226]    [Pg.108]    [Pg.649]    [Pg.129]    [Pg.100]    [Pg.338]    [Pg.258]    [Pg.210]    [Pg.161]    [Pg.161]    [Pg.505]    [Pg.56]    [Pg.255]    [Pg.7]    [Pg.370]    [Pg.345]   


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Dihydrobis borate as ligand in nickel complexes

Dihydrobis borate, reaction

Dihydrobis borate, reaction derivatives of tin

Potassium Dihydrobis(l-pyrazolyl)borate

Potassium dihydrobis borate

Potassium dihydrobis borate reaction with palladium complexes

Potassium dihydrobis borate reaction with ruthenium complexes

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