Heat of reaction of (norbornadiene) molybdenum tetracarbonyl with monodentate and bidentate ligands. Solution thermochemical study of ligand substitution in the complexes cis-L2Mo(CO)4

Shakti L. Mukerjee; Steven P. Nolan; Carl D. Hoff; Ramon Lopez de la Vega

doi:10.1021/ic00274a018

Heat of reaction of (norbornadiene) molybdenum tetracarbonyl with monodentate and bidentate ligands. Solution thermochemical study of ligand substitution in the complexes cis-L₂Mo(CO)₄

Shakti L. Mukerjee, Steven P. Nolan, Carl D. Hoff, Ramon Lopez de la Vega

Chemistry

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57 Scopus citations

Abstract

The enthalpy of reaction of (NBD)Mo(CO)₄ (NBD = norbornadiene) with a number of monodentate and bidentate ligands forming cis-L₂Mo(CO)₄ has been measured at 30°C in THF solution. The heats of reaction span a range of 33 kcal/mol. The order of stability for monodentate ligands is PCl₃ < As(C₆H₅)₃ < py < P(C₆H₅)₃ < AsEt₃ < P(OC₆H₅)₃ < P(C₆H₅)₂(CH₃) < CO < P(C₆H₅)(CH₃)₂ < P(OCH₃)₃ < P(n-Bu)₃ < (C₆H₁₁)NC < PEt₃ < PMe₃. The series of chelating bidentate phosphines R₂P-(CH₂)_nPR₂ (n = 1-4, R = C₆H₅; n = 1, 2, R = CH₃) and several related ligands were investigated. The chelating ring systems in the metallacycles show strain energies of about 8 kcal/mol for four-membered rings. The mixed ligand (C₆H₅)₂PCH₂CH₂-As(C ₆H₅)₂ shows a heat of binding midway between the heats of binding of (C₆H₅)₂PCH₂CH₂P(C ₆H₅)₂ and (C₆H₅)₂AsCH₂C-H₂As(C ₆H₅)₂, implying group additivity in this system. The complex (phen)Mo(CO)₄ is some 5 kcal/mol more stable than (bpy)Mo(CO)₄, presumably due to conformational effects in the free ligand. The ligand 1,5-cyclooctadiene forms a complex 2 kcal/mol less stable than that of norbornadiene. The influences of steric and electronic factors in determining the Mo-L bond strength are discussed.

Original language	English (US)
Pages (from-to)	81-85
Number of pages	5
Journal	Inorganic Chemistry
Volume	27
Issue number	1
DOIs	https://doi.org/10.1021/ic00274a018
State	Published - Jan 1 1988

ASJC Scopus subject areas

Physical and Theoretical Chemistry
Inorganic Chemistry

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Heat of reaction of (norbornadiene) molybdenum tetracarbonyl with monodentate and bidentate ligands. Solution thermochemical study of ligand substitution in the complexes cis-L₂Mo(CO)₄. / Mukerjee, Shakti L.; Nolan, Steven P.; Hoff, Carl D.; Lopez de la Vega, Ramon.

In: Inorganic Chemistry, Vol. 27, No. 1, 01.01.1988, p. 81-85.

Research output: Contribution to journal › Article › peer-review

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title = "Heat of reaction of (norbornadiene) molybdenum tetracarbonyl with monodentate and bidentate ligands. Solution thermochemical study of ligand substitution in the complexes cis-L2Mo(CO)4",

abstract = "The enthalpy of reaction of (NBD)Mo(CO)4 (NBD = norbornadiene) with a number of monodentate and bidentate ligands forming cis-L2Mo(CO)4 has been measured at 30°C in THF solution. The heats of reaction span a range of 33 kcal/mol. The order of stability for monodentate ligands is PCl3 < As(C6H5)3 < py < P(C6H5)3 < AsEt3 < P(OC6H5)3 < P(C6H5)2(CH3) < CO < P(C6H5)(CH3)2 < P(OCH3)3 < P(n-Bu)3 < (C6H11)NC < PEt3 < PMe3. The series of chelating bidentate phosphines R2P-(CH2)nPR2 (n = 1-4, R = C6H5; n = 1, 2, R = CH3) and several related ligands were investigated. The chelating ring systems in the metallacycles show strain energies of about 8 kcal/mol for four-membered rings. The mixed ligand (C6H5)2PCH2CH2-As(C 6H5)2 shows a heat of binding midway between the heats of binding of (C6H5)2PCH2CH2P(C 6H5)2 and (C6H5)2AsCH2C-H2As(C 6H5)2, implying group additivity in this system. The complex (phen)Mo(CO)4 is some 5 kcal/mol more stable than (bpy)Mo(CO)4, presumably due to conformational effects in the free ligand. The ligand 1,5-cyclooctadiene forms a complex 2 kcal/mol less stable than that of norbornadiene. The influences of steric and electronic factors in determining the Mo-L bond strength are discussed.",

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AU - Nolan, Steven P.

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AU - Lopez de la Vega, Ramon

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N2 - The enthalpy of reaction of (NBD)Mo(CO)4 (NBD = norbornadiene) with a number of monodentate and bidentate ligands forming cis-L2Mo(CO)4 has been measured at 30°C in THF solution. The heats of reaction span a range of 33 kcal/mol. The order of stability for monodentate ligands is PCl3 < As(C6H5)3 < py < P(C6H5)3 < AsEt3 < P(OC6H5)3 < P(C6H5)2(CH3) < CO < P(C6H5)(CH3)2 < P(OCH3)3 < P(n-Bu)3 < (C6H11)NC < PEt3 < PMe3. The series of chelating bidentate phosphines R2P-(CH2)nPR2 (n = 1-4, R = C6H5; n = 1, 2, R = CH3) and several related ligands were investigated. The chelating ring systems in the metallacycles show strain energies of about 8 kcal/mol for four-membered rings. The mixed ligand (C6H5)2PCH2CH2-As(C 6H5)2 shows a heat of binding midway between the heats of binding of (C6H5)2PCH2CH2P(C 6H5)2 and (C6H5)2AsCH2C-H2As(C 6H5)2, implying group additivity in this system. The complex (phen)Mo(CO)4 is some 5 kcal/mol more stable than (bpy)Mo(CO)4, presumably due to conformational effects in the free ligand. The ligand 1,5-cyclooctadiene forms a complex 2 kcal/mol less stable than that of norbornadiene. The influences of steric and electronic factors in determining the Mo-L bond strength are discussed.

AB - The enthalpy of reaction of (NBD)Mo(CO)4 (NBD = norbornadiene) with a number of monodentate and bidentate ligands forming cis-L2Mo(CO)4 has been measured at 30°C in THF solution. The heats of reaction span a range of 33 kcal/mol. The order of stability for monodentate ligands is PCl3 < As(C6H5)3 < py < P(C6H5)3 < AsEt3 < P(OC6H5)3 < P(C6H5)2(CH3) < CO < P(C6H5)(CH3)2 < P(OCH3)3 < P(n-Bu)3 < (C6H11)NC < PEt3 < PMe3. The series of chelating bidentate phosphines R2P-(CH2)nPR2 (n = 1-4, R = C6H5; n = 1, 2, R = CH3) and several related ligands were investigated. The chelating ring systems in the metallacycles show strain energies of about 8 kcal/mol for four-membered rings. The mixed ligand (C6H5)2PCH2CH2-As(C 6H5)2 shows a heat of binding midway between the heats of binding of (C6H5)2PCH2CH2P(C 6H5)2 and (C6H5)2AsCH2C-H2As(C 6H5)2, implying group additivity in this system. The complex (phen)Mo(CO)4 is some 5 kcal/mol more stable than (bpy)Mo(CO)4, presumably due to conformational effects in the free ligand. The ligand 1,5-cyclooctadiene forms a complex 2 kcal/mol less stable than that of norbornadiene. The influences of steric and electronic factors in determining the Mo-L bond strength are discussed.

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