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Pyridine thiocyanation

MiscelEneous. Small quantities of cobalt compounds are used in the production of electronic devices such as thermistors, varistors, piezoelectrics (qv), and solar collectors. Cobalt salts are useful indicators for humidity. The blue anhydrous form becomes pink (hydrated) on exposure to high humidity. Cobalt pyridine thiocyanate is a useful temperature indicating salt. A conductive paste for painting on ceramics and glass is composed of cobalt oxide (62). [Pg.382]

Trichlorotellurium sulfonates form coordination compounds with sulfonates, pyridine, thiocyanate and oxo groups as ligands1. [Pg.97]

Epoxy-17a-pregnan-20-ones react with pyridine thiocyanate to give thiocyano-alcohols, which readily cyclize to afford cyclic thiocarbonates (51). ... [Pg.240]

PROPERTIES AND DERIVATIVES. Germidine, Cj4H6 OioN, is dimorphic and melts at 198-200° or 230-231° (dec.) (dil. ethanol) [a]o + 13 (chloroform), —11° (pyridine) thiocyanate, m.p. 242-244 (dec.) (dil. methanol). Alkaline hydrolysis of germidine gave rise to germine and a mixture of acetic and d-(—)-a-methylbutyric acid, which were obtained in the form of their p-phenylphenacyl esters (19). [Pg.275]

Probably first obtained by Hantzsch and Arapides (105) by condensation of a,/3-dichlorether with barium thiocyanate, and identified by its pyridine-like odor, thiazole was first prepared in 1889 by G. Popp (104) with a yield of 10% by the reduction in boiling ethanol of thiazol-2-yldiazonium sulfate resulting from the diazotization of 2-aminothiazole. prepared the year before by Traumann (103). The unique cyclization reaction affording directly the thiazole molecule was described in 1914 by Gabriel and Bachstez (106). They applied the method of cyclization, developed by Gabriel (107, 108), to the diethylacetal of 2-formylamino-ethanal and obtained thiazole with a yield of 62% - Thiazole was also formed in the course of a study on the ease of decarboxylation of the three possible monocarboxylic acids derived from it (109). On the other... [Pg.24]

Pyridine plus thiocyanate Dilute acid solution. Ag, Cd, Cu, Mn, Ni... [Pg.1145]

Chloro-a,/3-unsaturated aldehydes condense with ammonium thiocyanate to give isothiazoles (76EGP122249). 2,3-Diphenylcyclopropenone reacts with iV-sulfinyl-cyclohexylamine in the presence of nickel tetracarbonyl to give the isothiazolin-3-one 1-oxide (197) (79SST(5)345). Cholesteryl acetate reacts with trithiazyl trichloride in pyridine to give the isothiazolo steroid (198) (77JCS(P1)916). [Pg.169]

The [Ni(NCS)f,]4 ion is almost perfectly octahedral, with Ni—N distances of around 209.5 pm and N—Ni—N angles around 89.5°. The Ni—N—C and N—C—S entities are practically linear.438,439 In [Ni(NCS)2L2] where L is a R-substituted pyridine, stereochemistry and spin state depend on the type and positions of R.431 While for 2-Me- and 2-Et-pyridine square planar complexes are observed, other pyridins lead to coordination polymers with pseudo-octahedral Ni11 due to N,S-bridging thiocyanate. Ni11 thiocyanato complexes have been studied quite intensively as hosts for inclusion compounds.440"442... [Pg.283]

Pyridine derivatives with additional donor functions and sterically demanding substituents have been used with the intention of producing complexes of Cd (and of other metals) with low coordination number one of these ligands is the tridentate, planar-bonding 2,6-bis[(2,6-dimethyl-phenylimino)methyl] pyridine (pydim a Schiff base derived from 2,6-pyridine dialdehyde), which with Cd(BF4)2 and thiocyanate gives a dinuclear complex [(pydim)Cd(/x-NCS-S,N)]2(BF4)2 with N-dominated coordination sphere.191 As centrosymmetric Plijc, Z= 2), the complex has an antiparallel /x-1,3 NCS double bridge with Cd—N and Cd—S bonds (224.6 pm and 255.5 pm, respectively) the Cd—N(py) bond is clearly shorter than the Cd—N(imino) bonds (225.6 pm and 245.0 pm,... [Pg.1271]

High density brine completion fluids also often require the use of corrosion inhibitors (8,9). Blends of thioglycolates and thiourea alkyl, alkenyl, or alkynyl phosphonium salts thiocyanate salts mercaptoacetic acid and its salts and the reaction products of pyridine or pyrazine derivatives with dicarboxylic acid monoanhydrides have been used as high density brine corrosion inhibitors. [Pg.23]

Plasma Deproteinization with trichloroacetic acid bromination of supernatant and treatment with pyridine-p-phenylene diamine Spectrophotometry (thiocyanate- cyanide determination) 0.07 ppm 96 (thiocyanate) Pettigrew and Fell 1972... [Pg.195]


See other pages where Pyridine thiocyanation is mentioned: [Pg.460]    [Pg.109]    [Pg.283]    [Pg.276]    [Pg.125]    [Pg.134]    [Pg.70]    [Pg.460]    [Pg.109]    [Pg.283]    [Pg.276]    [Pg.125]    [Pg.134]    [Pg.70]    [Pg.329]    [Pg.170]    [Pg.786]    [Pg.501]    [Pg.203]    [Pg.101]    [Pg.77]    [Pg.78]    [Pg.111]    [Pg.115]    [Pg.131]    [Pg.137]    [Pg.149]    [Pg.160]    [Pg.210]    [Pg.232]    [Pg.244]    [Pg.252]    [Pg.284]    [Pg.453]    [Pg.479]    [Pg.725]    [Pg.941]    [Pg.742]    [Pg.1414]    [Pg.331]    [Pg.608]    [Pg.302]   
See also in sourсe #XX -- [ Pg.252 ]




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Nickel pyridine thiocyanate

Pyridine thiocyanates

Zinc pyridine thiocyanate

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