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일반 설명
Boron triiodide is a strong Lewis acid. It can be prepared by treating iodine (I2) with potassium borohydride (KBH4) in heptane.
애플리케이션
Boron triiodide can be used as a reagent to cleave C-O bonds in ethers, esters, and alcohols. It can also be used to cleave silanes and halides. Boron triiodide converts alcohols to alkyl iodides; sulfonyl and sulfinyl to disulfides. Borylation of triarylamines can be achievd using this reagent.
It can also be used to prepare imidazole based imino aluminum dihalide metal complexes and boron carbonitride (BCN) nanowires.
It can also be used to prepare imidazole based imino aluminum dihalide metal complexes and boron carbonitride (BCN) nanowires.
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
이미 열람한 고객
Boron Triiodide
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Multiple Electrophilic C-H Borylation of Arenes Using Boron Triiodide
Organic Letters, 22(2), 700-704 (2020)
Synthesis, characterization and reactivity of an imidazolin-2-iminato aluminium dihydride
Dalton Transactions, 43(11), 4451-4461 (2014)
Synthesis and growth mechanism of BCN nanowires
Materials Letters, 65(15-16), 2476-2478 (2011)
Dalton transactions (Cambridge, England : 2003), 43(11), 4451-4461 (2013-12-18)
The reaction of bis(2,6-diisopropylphenyl)imidazolin-2-imine (LH, 1) with Me3N·AlH3 furnishes {μ-LAlH2}2 (2). The marked tendency of 2 to release its hydride substituents is ascribed to the strong electron-donor character of the imidazolin-2-iminato ligand. This is supported by its reactivity study and
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