76782-93-9

Upstream product

• 253185-03-4 tert-butylbenzene 
• 10294-33-4 boron tribromide 
• 19287-45-7 diborane 
• 3972-65-4 1-bromo-4-tert-butylbenzene 
• 18412-68-5 (4-tert-butylphenyl)trimethylsilane 

Downstream Products

• 1383486-17-6 t-butylphenyl dibromoborane 
• 1449251-15-3 C₅₀H₅₀B₂MgN₆ 
• 1233483-06-1 ((C₉H₅N)(O)((C₆H₄)N(CH₃)2))B((C₆H₄)CHCH₂)((C₆H₄)C(CH₃)3) 
• 1233483-05-0 ((C₉H₆N)(O))B((C₆H₄)CHCH₂)((C₆H₄)C(CH₃)3) 
• 1082577-50-1 t-BuC₆H₄(St)BBr 
• 1210318-31-2 sodium tris(pentafluorophenyl)(t-butylphenyl)borate 
• 923001-29-0 5,5'-bis-[bis-(4-tert-butyl-phenyl)-boranyl]-[2,2']bithiophenyl 

Relevant academic research and scientific papers

RAFT polymerization of luminescent boron quinolate monomers

Fluorescent homopolymers and amphiphilic block copolymers were prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization of two new styryl-type organoboron monomers; the fluorescence characteristics of PEO block copolymers in aque

Luminescence tuning of organoboron quinolates through substituent variation at the 5-position of the quinolato moiety

A series of organoboron quinolates with emission colors ranging from blue to red have been prepared. In comparison to the respective AlQ3 derivatives a distinct blue-shift of the emission is observed. Theoretical calculations serve to provide i

A New Borylation Method for Alkylbenzene and Polystyrene

The borylation of alkylbenzenes by Hal2BH (Hal = F, Cl, Br) gives H2 and a mixture of m- and p-alkyl(dihaloboryl)benzenes.In the case of bulky alkyl groups, such as isopropyl, tert-butyl, these are partially split off as R - H and RBHal2.The phenyl groups in polystyrene-divinylbenzene copolymers undergo borylation with Br2BH in a 55percent yield.