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dc.contributor.authorKagwanja, Stanley M.
dc.contributor.authorJeffery, John C.
dc.contributor.authorJohns, Christopher J.
dc.contributor.authorMcCleverty, John A.
dc.date.accessioned2020-02-06T13:46:41Z
dc.date.available2020-02-06T13:46:41Z
dc.date.issued1996-06
dc.identifier.citationElsevier Polyhedron Volume 15, Issue 17, June 1996, Pages 2959-2967en_US
dc.identifier.urihttp://repository.chuka.ac.ke/handle/chuka/611
dc.description.abstractThe reaction of 2 mol equiv. of [Mo(NO){HB(dmpz)3}X2] ((HBdmpz)3 = tris(3,5-dimethylpyrazolyl)borate; X = Cl or I) with Schiff base ligands derived by condensation of 2 mol equiv. of para- and meta-hydroxybenzaldehyde with 1,4-C6H4(NH2)2 and 1,6-NH2(CH2)6NH2 afforded monometallic complexes [Mo(NO) {H(dmpz3)} X(OC6H4 CHO)]. Sodium borohydride reduction of the Schiff bases obtained from the hydroxybenzaldehydes and 1,4-C6H4(NH2)2 followed by reaction with [Mo(NO){HB(dmpz)3 Cl2}] afforded the bimetallic species [{Mo(NO)HB(dmpz)3}Cl{(OC6H4CH2NH)2C6H4}]. These compounds were characterized spectroscopically and the structure of a closely related compound, [Mo(NO){HB(dmpz)3}Cl{OC6H3(3-CHO)(4-OH)}], has been determined crystallographically.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.titleReaction of molybdenum mononitrosyl halides with Schiff bases: Hydrolysis of azomethine links,formation of monometallic trisen_US
dc.typeArticleen_US


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