Borane carbonyl

Borane carbonyl
Names
	Other names Carbonyltrihydroboron
Identifiers
CAS Number	13205-44-2;
ChemSpider	10225684;
Properties
Chemical formula	CH3BO
Molar mass	41.84 g·mol−1
Appearance	colorless gas
Density	1.71 g/L[1]
Melting point	−137[1] °C (−215 °F; 136 K)
Boiling point	−64[1] °C (−83 °F; 209 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Borane carbonyl is the inorganic compound with the formula H₃BCO. This colorless gas is the adduct of borane and carbon monoxide. It is usually prepared by combining borane-ether complexes and CO. The compound is mainly of theoretical and pedagogical interest.[2] It reacts with aqueous base to give boranocarbonate H₃BCO₂²⁻.[3] Bond distances are B−C, 1.529; C−O, 1.140; 1.194 Å. The H−B−H angle is 113.7°. The CO vibrational band is at 2165 cm⁻¹, 22 cm⁻¹ higher than that of free CO.[4]

References

www.chemicalbook.com https://www.chemicalbook.com/ChemicalProductProperty_EN_CB72358168.htm. Missing or empty |title= (help)
Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 165. ISBN 978-0-08-037941-8.
Alberto, R.; Ortner, K.; Wheatley, N.; Schibli, R.; Schubiger, A. P. (2001). "Synthesis and Properties of Boranocarbonate: A Convenient in Situ CO Source for the Aqueous Preparation of [^99mTc(OH₂)₃(CO)₃]⁺". J. Am. Chem. Soc. 123: 3135–3136. doi:10.1021/ja003932b. PMID 11457025.CS1 maint: uses authors parameter (link)
Jacobsen, H.; Berke, H.; Doering, S.; Kehr, G.; Erker, G.; Froehlich, R.; Meyer, O. (1999). "Lewis Acid Properties of Tris(pentafluorophenyl)borane. Structure and Bonding in L-B(C₆F₅)₃ Complexes". Organometallics. 18: 1724–1735. doi:10.1021/OM981033E.CS1 maint: uses authors parameter (link)

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[ChemBook-1] www.chemicalbook.com https://www.chemicalbook.com/ChemicalProductProperty_EN_CB72358168.htm. Missing or empty |title= (help)

[2] Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 165. ISBN 978-0-08-037941-8.

[3] Alberto, R.; Ortner, K.; Wheatley, N.; Schibli, R.; Schubiger, A. P. (2001). "Synthesis and Properties of Boranocarbonate: A Convenient in Situ CO Source for the Aqueous Preparation of [^99mTc(OH₂)₃(CO)₃]⁺". J. Am. Chem. Soc. 123: 3135–3136. doi:10.1021/ja003932b. PMID 11457025.CS1 maint: uses authors parameter (link)

[4] Jacobsen, H.; Berke, H.; Doering, S.; Kehr, G.; Erker, G.; Froehlich, R.; Meyer, O. (1999). "Lewis Acid Properties of Tris(pentafluorophenyl)borane. Structure and Bonding in L-B(C₆F₅)₃ Complexes". Organometallics. 18: 1724–1735. doi:10.1021/OM981033E.CS1 maint: uses authors parameter (link)