![]() | |
![]() | |
Names | |
---|---|
Preferred IUPAC name
Triphenylborane | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.012.277 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C18H15B | |
Molar mass | 242.12 g/mol |
Appearance | White crystals |
Melting point | 142 °C (288 °F; 415 K) |
Boiling point | 203 °C (397 °F; 476 K) (15 mmHg) |
Insoluble | |
Structure | |
trigonal planar | |
Hazards | |
GHS labelling: | |
![]() | |
Warning | |
H228 | |
P210, P240, P241, P280, P370+P378 | |
Related compounds | |
Related
isoelectronic
|
Triphenylmethyl cation |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Triphenylborane, often abbreviated to BPh3 where Ph is the phenyl group C6H5-, is a chemical compound with the formula B(C6H5)3. It is a white crystalline solid and is both air and moisture sensitive, slowly forming benzene and triphenylboroxine. It is soluble in aromatic solvents.
The core of the compound, BC3, has a trigonal planar structure. The phenyl groups are rotated at about a 30° angle from the core plane. [1]
Even though triphenylborane and tris(pentafluorophenyl)borane are structurally similar, their Lewis acidity is not. BPh3 is a weak Lewis acid while B(C6F5)3 is a strong Lewis acid due to the electronegativity of the fluorine atoms. Other boron Lewis acids include BF3 and BCl3. [2]
Triphenylborane was first synthesized in 1922. [3] It is typically made with boron trifluoride diethyl etherate and the Grignard reagent, phenylmagnesium bromide. [4]
Triphenylborane can also be synthesized on a smaller scale by the thermal decomposition of trimethylammonium tetraphenylborate. [5]
Triphenylborane is made commercially by a process developed by Du Pont for use in its hydrocyanation of butadiene to adiponitrile, a nylon intermediate. Du Pont produces triphenylborane by reacting sodium metal, a haloaromatic ( chlorobenzene), and a secondary alkyl borate ester. [6]
Triphenylborane can be used to make triarylborane amine complexes, such as pyridine-triphenylborane. Triarylborane amine complexes are used as catalysts for the polymerization of acrylic esters. [6]
{{
cite book}}
: |journal=
ignored (
help)
![]() | |
![]() | |
Names | |
---|---|
Preferred IUPAC name
Triphenylborane | |
Identifiers | |
3D model (
JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.012.277 |
EC Number |
|
PubChem
CID
|
|
UNII | |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C18H15B | |
Molar mass | 242.12 g/mol |
Appearance | White crystals |
Melting point | 142 °C (288 °F; 415 K) |
Boiling point | 203 °C (397 °F; 476 K) (15 mmHg) |
Insoluble | |
Structure | |
trigonal planar | |
Hazards | |
GHS labelling: | |
![]() | |
Warning | |
H228 | |
P210, P240, P241, P280, P370+P378 | |
Related compounds | |
Related
isoelectronic
|
Triphenylmethyl cation |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
Triphenylborane, often abbreviated to BPh3 where Ph is the phenyl group C6H5-, is a chemical compound with the formula B(C6H5)3. It is a white crystalline solid and is both air and moisture sensitive, slowly forming benzene and triphenylboroxine. It is soluble in aromatic solvents.
The core of the compound, BC3, has a trigonal planar structure. The phenyl groups are rotated at about a 30° angle from the core plane. [1]
Even though triphenylborane and tris(pentafluorophenyl)borane are structurally similar, their Lewis acidity is not. BPh3 is a weak Lewis acid while B(C6F5)3 is a strong Lewis acid due to the electronegativity of the fluorine atoms. Other boron Lewis acids include BF3 and BCl3. [2]
Triphenylborane was first synthesized in 1922. [3] It is typically made with boron trifluoride diethyl etherate and the Grignard reagent, phenylmagnesium bromide. [4]
Triphenylborane can also be synthesized on a smaller scale by the thermal decomposition of trimethylammonium tetraphenylborate. [5]
Triphenylborane is made commercially by a process developed by Du Pont for use in its hydrocyanation of butadiene to adiponitrile, a nylon intermediate. Du Pont produces triphenylborane by reacting sodium metal, a haloaromatic ( chlorobenzene), and a secondary alkyl borate ester. [6]
Triphenylborane can be used to make triarylborane amine complexes, such as pyridine-triphenylborane. Triarylborane amine complexes are used as catalysts for the polymerization of acrylic esters. [6]
{{
cite book}}
: |journal=
ignored (
help)