Movatterモバイル変換


[0]ホーム

URL:


Jump to content
WikipediaThe Free Encyclopedia
Search

Diboron tetrachloride

From Wikipedia, the free encyclopedia
Diboron tetrachloride
Names
Preferred IUPAC name
Diboron tetrachloride
Systematic IUPAC name
Tetrachlorodiborane(4)
Identifiers
3D model (JSmol)
ChemSpider
UNII
  • InChI=1S/B2Cl4/c3-1(4)2(5)6
    Key: LCWVIHDXYOFGEG-UHFFFAOYSA-N
  • InChI=1S/B2Cl4/c3-1(4)2(5)6
    Key: LCWVIHDXYOFGEG-UHFFFAOYAN
  • ClB(Cl)B(Cl)Cl
Properties
B2Cl4
Molar mass163.42 g·mol−1
Appearancecolorless liquid
Density1.5 g/cm3 (0 °C)
Melting point−92.6 °C (−134.7 °F; 180.6 K)
Boiling point65.5 °C (149.9 °F; 338.6 K)
Thermochemistry
137.7 J/mol K
232.3 J/mol K
−523 kJ/mol
−468.8 kJ/mol
Related compounds
Related compounds
Diboron tetrafluoride
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Diboron tetrachloride is atetrahalodiboranechemical compound with theformula B2Cl4. It is a colorless liquid.[1]

Synthesis

[edit]

The modern synthesis involves the chlorination ofdiboron tetrabromide bygallium(III) chloride.[2]

It can also be formed by the electricaldischarge procedure of boron trichloride at low temperatures:[1][3]

BCl3 → BCl2 + Cl
Cl + Hg (electrode) → Hg2Cl2 or HgCl2
2 BCl2 → B2Cl4

The most efficient synthesis technique uses no dechlorinating metal, instead passingradio-frequencyAC current through gaseous boron trichloride.[4]

Structure

[edit]

The molecular structure of diboron tetrachloride, B2Cl4, was determined bygas electron diffraction.[5] The molecules haveD2dsymmetry, i.e. the two planar BBCl2 units are perpendicular to each other (torsion angle Cl-B-B-Cl 90°). The B-B distance is 1.70(4) Å, the B-Cl distance is 1.750(5) Å, the Cl-B-Cl angle is 118.7(3)°. B2Cl4 thus differs significantly fromB2F4, which is a planar molecule overall.

Structure of B2Cl4 in the gas phase as determined by gas electron diffraction

Reactions

[edit]

The compound is used as areagent for the synthesis oforganoboron compounds. For instance, diboron tetrachlorideadds toethylene:[6]

CH2=CH2 + B2Cl4 → Cl2B–CH2–CH2–BCl2

Diboron tetrachloride absorbshydrogen quickly atroom temperature:[3]

3 B2Cl4 + 3 H2 → B2H6 + 4 BCl3

Withboranes, it replaces a hydrogen to form dichloroborane(3) and a polyhedral dichloroborane. Heat inducesdisproportionation back toboron trichloride and a polyhedral boron(I) chloride.[4]

References

[edit]
  1. ^abP. L. Timms (1972). "Low Temperature Condensation".Advances in Inorganic Chemistry and Radiochemistry. Academic Press. p. 143.ISBN 0-12-023614-1.
  2. ^Merle Arrowsmith; Julian Böhnke; Holger Braunschweig; Andrea Deißenberger; Rian D. Dewhurst; William C. Ewing; Christian Hörl; Jan Miesa; Jonas H. Muessig (2017). "Simple solution-phase syntheses of tetrahalodiboranes(4) and their labile dimethylsulfide adducts".Chemical Communications (59).doi:10.1039/C7CC03148C.
  3. ^abUrry, Grant; Wartik, Thomas; Moore, R. E.; Schlesinger, H. I. (1954). "The Preparation and Some of the Properties of Diboron Tetrachloride, B2Cl4".Journal of the American Chemical Society.76 (21):5293–5298.doi:10.1021/ja01650a010.ISSN 0002-7863.
  4. ^abMorrison, John A. (1991-01-01)."Chemistry of the polyhedral boron halides and the diboron tetrahalides".Chemical Reviews.91 (1):35–48.doi:10.1021/cr00001a003.ISSN 0009-2665.
  5. ^Ryan, Robert R.; Hedberg, Kenneth (1969-06-01)."Effect of Temperature on the Structure of Gaseous Molecules. II. An Electron‐Diffraction Investigation of the Molecular Structures of B2Cl4 and SiCl4. The Potential Function for Internal Rotation in B2Cl4".The Journal of Chemical Physics.50 (11):4986–4995.doi:10.1063/1.1670995.ISSN 0021-9606.
  6. ^Urry, Grant; Kerrigan, James; Parsons, Theran D.; Schlesinger, H. I. (1954). "Diboron Tetrachloride, B2Cl4, as a Reagent for the Synthesis of Organo-boron Compounds. I. The Reaction of Diboron Tetrachloride with Ethylene".Journal of the American Chemical Society.76 (21):5299–5301.doi:10.1021/ja01650a011.ISSN 0002-7863.
Boron pnictogenides
Boron halides
Acids
Boranes
Boron oxides and sulfides
Carbides
Organoboron compounds
Salts and covalent derivatives of thechloride ion
HClHe
LiClBeCl2B4Cl4
B12Cl12
BCl3
B2Cl4
+BO3
C2Cl2
C2Cl4
C2Cl6
CCl4
+C
+CO3
NCl3
ClN3
+N
+NO3
ClxOy
Cl2O
Cl2O2
ClO
ClO2
Cl2O4
Cl2O6
Cl2O7
ClO4
+O
ClF
ClF3
ClF5
Ne
NaClMgCl2AlCl
AlCl3
Si5Cl12
Si2Cl6
SiCl4
P2Cl4
PCl3
PCl5
+P
S2Cl2
SCl2
SCl4
+SO4
Cl2Ar
KClCaCl
CaCl2
ScCl3TiCl2
TiCl3
TiCl4
VCl2
VCl3
VCl4
VCl5
CrCl2
CrCl3
CrCl4
MnCl2
MnCl3
FeCl2
FeCl3
CoCl2
CoCl3
NiCl2CuCl
CuCl2
ZnCl2GaCl
GaCl3
GeCl2
GeCl4
AsCl3
AsCl5
+As
Se2Cl2
SeCl2
SeCl4
BrClKr
RbClSrCl2YCl3ZrCl2
ZrCl3
ZrCl4
NbCl3
NbCl4
NbCl5
MoCl2
MoCl3
MoCl4
MoCl5
MoCl6
TcCl3
TcCl4
RuCl2
RuCl3
RuCl4
RhCl3PdCl2AgClCdCl2InCl
InCl2
InCl3
SnCl2
SnCl4
SbCl3
SbCl5
Te3Cl2
TeCl2
TeCl4
ICl
ICl3
XeCl
XeCl2
XeCl4
CsClBaCl2*LuCl3
177LuCl3
HfCl4TaCl3
TaCl4
TaCl5
WCl2
WCl3
WCl4
WCl5
WCl6
ReCl3
ReCl4
ReCl5
ReCl6
OsCl2
OsCl3
OsCl4
OsCl5
IrCl2
IrCl3
IrCl4
PtCl2
PtCl4
PtCl2−6
AuCl
(Au[AuCl4])2
AuCl3
AuCl4
Hg2Cl2
HgCl2
TlCl
TlCl3
PbCl2
PbCl4
BiCl3PoCl2
PoCl4
AtClRn
FrClRaCl2**LrCl3RfCl4DbCl5SgO2Cl2BhO3ClHsMtDsRgCnNhFlMcLvTsOg
 
*LaCl3CeCl3PrCl3NdCl2
NdCl3
PmCl3SmCl2
SmCl3
EuCl2
EuCl3
GdCl3TbCl3DyCl2
DyCl3
HoCl3ErCl3TmCl2
TmCl3
YbCl2
YbCl3
**AcCl3ThCl3
ThCl4
PaCl4
PaCl5
UCl3
UCl4
UCl5
UCl6
NpCl3
NpCl4
PuCl3
PuCl4
PuCl2−6
AmCl2
AmCl3
CmCl3BkCl3CfCl3
CfCl2
EsCl2
EsCl3
FmCl2MdCl2NoCl2


Stub icon

Thisinorganiccompound–related article is astub. You can help Wikipedia byexpanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Diboron_tetrachloride&oldid=1297126804"
Categories:
Hidden categories:

[8]ページ先頭

©2009-2025 Movatter.jp