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Volumn 112, Issue 50, 2008, Pages 12896-12903

Pd-catalyzed homocoupling reaction of arylboronic acid: Insights from density functional theory

Author keywords

[No Author keywords available]

Indexed keywords

ACIDS; ATOMIC PHYSICS; BORON; BORON COMPOUNDS; COORDINATION REACTIONS; DENSITY FUNCTIONAL THEORY; ISOMERIZATION; OXYGEN; PALLADIUM;

EID: 84962477033     PISSN: 10895639     EISSN: None     Source Type: Journal    
DOI: 10.1021/jp801948u     Document Type: Article
Times cited : (36)

References (58)
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    • Basis-set superposition errors were evaluated by using the standard Counterpoise correction, the largest being of the order of 6 kcal/mol. To test basis-set dependence of energetic and structural features, additional calculations were performed by using a larger basis set only on O, P, and B atoms in order to test basis-set dependence for the formation of 2. In particular, it was shown that the same qualitative results are obtained with a Pople triple-zeta basis including polarization function on these atoms (6-311G(d)). The same holds when adding a diffuse function on oxygen atoms (i.e. 6-311+G(d)). Therefore, if not differently specified, all values correspond to those obtained with the LANL2DZ basis.
    • Basis-set superposition errors were evaluated by using the standard Counterpoise correction, the largest being of the order of 6 kcal/mol. To test basis-set dependence of energetic and structural features, additional calculations were performed by using a larger basis set only on O, P, and B atoms in order to test basis-set dependence for the formation of 2. In particular, it was shown that the same qualitative results are obtained with a Pople triple-zeta basis including polarization function on these atoms (6-311G(d)). The same holds when adding a diffuse function on oxygen atoms (i.e. 6-311+G(d)). Therefore, if not differently specified, all values correspond to those obtained with the LANL2DZ basis.
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    • For hypothetical reactions of ArPd(OH)L2 with arylboronic acids, see ref 2c
    • 2 with arylboronic acids, see ref 2c.
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    • For reactions and kinetic data, see, unpublished results
    • (b) For reactions and kinetic data, see Amatore, C.; Boubekeur-Lecaque, L.; Jutand, A. 2008, unpublished results,
    • (2008)
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  • 58
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    • Even if all experiments have been performed in anhydrous conditions, the presence of water cannot be excluded because of the equilibrium between arylboronic acid and its boroxine
    • Even if all experiments have been performed in anhydrous conditions, the presence of water cannot be excluded because of the equilibrium between arylboronic acid and its boroxine.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.