organoborane

(redirected from Organoboron)

organoborane

[ȯr¦gan·ə′bȯr‚ān]
(organic chemistry)
A derivative of a borane (boron hydride) in which one or more hydrogen atoms have been replaced by functional groups.
References in periodicals archive ?
The kind of that flame retardants is versatile, which mainly include organophosphorus [5-8], organosilicon [9-12], organoboron [13, 14], organonitrogen [15, 16], and other organometallic transition compounds [17, 18].
Synthesis of an E-BODIPY based fluorescent Co-polymer containing organoboron quinolate units.
Recent studies show that potassium organotrifluor-oborates are effective organoboron reagents for various organic transformations.
Albemarle's market leading technologies include metal organics, organoboron activators, electron donors, metallocenes, Ziegler PE and supported metallocene PE and PP catalysts.
Albemarle's market leading technologies include metal alkyls, MAO and organoboron co-catalysts, electron donors, metallocenes, Ziegler PE and supported metallocene PE & PP catalysts.
His research program encompasses the development of new organic reactions, catalysis, organoboron chemistry, the synthesis of alkaloid natural products and other heterocycles, and their application in probing cellular processes and as anticancer agents.
AllyChem, a major organoboron chemical manufacturer located in Dalian, China, will offer its customers a label license where purchasers have a royalty-free license to the University of Illinois' intellectual property in use of the MIDA boronates.
Highly luminescent BODIPY-based organoboron polymer exhibiting supramolecular self-assemble structure.
Three different organoboron compounds, boronic acid, boronate, and trifluoroborate, containing pyrrole were synthesized and then used in cross-coupling reactions with iodoanisole, bromoanisole, iodobenzene, and bromo-benze to assess the reactivity of the organoboron compounds and their potential as reagents in the synthesis of pentabromopseudilin.
The conjugated organoboron polymers have been synthesized in recent years [6].
The Monday afternoon session focussed on chain extenders for polyesters and nylon-6, novel poly(methylenephosphine)s and poly(p-phenylenephosphaalkenes, fluorescent materials based on phosphaoligothiophenes, linear and hyperbranched polymers bearing 1,2,3,4,5-pentaphenylsilolyl groups, hybrid resins containing polyhedral oligomeric silsesquioxanes, the use of Wilkinson's catalyst in silane dehydrocoupling reactions, Lewis acidic organoboron derivatives of polystyrene, and ruthenium macrocycles.