모든 사진(2)
About This Item
Linear Formula:
(C6F5)3B
CAS Number:
Molecular Weight:
511.98
MDL number:
UNSPSC 코드:
12352103
PubChem Substance ID:
NACRES:
NA.23
추천 제품
![Sodium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate](/deepweb/assets/sigmaaldrich/product/structures/251/439/7a621e74-bfd1-4a43-833c-09adfcc1e0b3/640/7a621e74-bfd1-4a43-833c-09adfcc1e0b3.png)
Quality Level
분석
95%
형태
powder
환경친화적 대안 제품 특성
Catalysis
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mp
126-131 °C (lit.)
환경친화적 대안 카테고리
SMILES string
Fc1c(F)c(F)c(B(c2c(F)c(F)c(F)c(F)c2F)c3c(F)c(F)c(F)c(F)c3F)c(F)c1F
InChI
1S/C18BF15/c20-4-1(5(21)11(27)16(32)10(4)26)19(2-6(22)12(28)17(33)13(29)7(2)23)3-8(24)14(30)18(34)15(31)9(3)25
InChI key
OBAJXDYVZBHCGT-UHFFFAOYSA-N
일반 설명
B(C6F5)3 is a Lewis acid, stronger than the inorganic parent molecule BF3. In contrast to the prominent Lewis acids, the pentafluorides of the heavier elements of group 15, B(C6F5)3 has no oxidizing properties. B(C6F5)3 forms adducts with neutral and weaker Lewis bases. B(C6F5)3 has the capability to easily accept anionic ligands bonded to metals.
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애플리케이션
A versatile reagent widely used in the preparation of d0 arene and other organometallic complexes useful as polymerization catalysts.
Used with tri-tert-butylphosphine (570958) to study the heterolytic cleavage of dihydrogen at room temperature and one atmosphere pressure.
Used with tri-tert-butylphosphine (570958) to study the heterolytic cleavage of dihydrogen at room temperature and one atmosphere pressure.
특징 및 장점
A versatile reagent widely used in the preparation of d0 arene and other organometallic complexes useful as polymerization catalysts.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
dust mask type N95 (US), Eyeshields, Gloves
이미 열람한 고객
![Potassium tetrakis[3,5-bis(trifluoromethyl)phenyl]borate Selectophore™](/deepweb/assets/sigmaaldrich/product/structures/631/130/b5486f44-2e69-40d0-902f-dd71894a6add/640/b5486f44-2e69-40d0-902f-dd71894a6add.png)
Hans Fuhrmann et al.
Inorganic chemistry, 35(23), 6742-6745 (1996-11-06)
The reaction of trimethylsilyl-substituted 2-aminopyridines with mixed chloro(dialkylamido)metal complexes (titanium and zirconium) leads via amine elimination to octahedral group 4 metal complexes that contain amine, amido, and aminopyridinato ligands. The X-ray crystal structure analyses of (4-Me-TMS-APy)(NMe(2))(HNMe(2))TiCl(2) (1) (crystallographic data: P2(1)/c
Organometallics, 15, 3600-3600 (1996)
Facile heterolytic cleavage of dihydrogen by phosphines and boranes.
Gregory C Welch et al.
Journal of the American Chemical Society, 129(7), 1880-1881 (2007-01-31)
Journal of the American Chemical Society, 118, 10008-10008 (1996)
Berthold Wegner et al.
Advanced science (Weinheim, Baden-Wurttemberg, Germany), 7(17), 2001322-2001322 (2020-10-01)
Molecular doping allows enhancement and precise control of electrical properties of organic semiconductors, and is thus of central technological relevance for organic (opto-) electronics. Beyond single-component molecular electron acceptors and donors, organic salts have recently emerged as a promising class
문서
The properties of many devices are limited by the intrinsic properties of the materials that compose them.
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