Publication: Experimental and computational exploration of the dynamic behavior of (PNP)BF<inf>2</inf>, a boron compound supported by an amido/bis(phosphine) pincer ligand
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Issued Date
2011-11-21
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14779234
14779226
14779226
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2-s2.0-80054970515
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Mahidol University
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SCOPUS
Bibliographic Citation
Dalton Transactions. Vol.40, No.43 (2011), 11562-11570
Suggested Citation
Jessica C. Demott, Panida Surawatanawong, Shoshanna M. Barnett, Chun Hsing Chen, Bruce M. Foxman, Oleg V. Ozerov Experimental and computational exploration of the dynamic behavior of (PNP)BF<inf>2</inf>, a boron compound supported by an amido/bis(phosphine) pincer ligand. Dalton Transactions. Vol.40, No.43 (2011), 11562-11570. doi:10.1039/c1dt11172h Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/11687
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Title
Experimental and computational exploration of the dynamic behavior of (PNP)BF<inf>2</inf>, a boron compound supported by an amido/bis(phosphine) pincer ligand
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Abstract
The diarylamido/bis(phosphine) PNP pincer ligand (2- i Pr 2 P-4-MeC 6 H 3 ) 2 N has been evaluated as a scaffold for supporting a BF 2 fragment. Compound (PNP)BF 2 (6) was prepared by simple metathesis of (PNP)Li (5) with Me 2 SBF 3 . NMR spectra of 6 in solution are of apparent C 2 symmetry, suggestive of a symmetric environment about boron. However, a combination of X-ray structural studies, low-temperature NMR investigations, and DFT calculations consistently establish that the ground state of this molecule contains a classical four-coordinate boron with a PNBF 2 coordination environment, with one phosphine donor in PNP remaining "free". Fortuitous formation of a single crystal of (PNP)BF 2 ·HBF 4 (7), in which the "free" phosphine is protonated, furnished another structure containing the same PNBF 2 environment about boron for comparison and the two PNBF 2 environments in 6 and 7 are virtually identical. DFT studies on several other diarylamido/bis(phosphine) pincer (PNP)BF 2 systems were carried out and all displayed a similar four coordinate PNBF 2 environment in the ground state structures. The symmetric appearance of the room-temperature NMR spectra is explained by the rapid interconversion between two degenerate four-coordinate, C 1 -symmetric ground-state forms. Lineshape analysis of the 1 H and 19 F NMR spectra over a temperature range of 180-243 K yielded the activation parameters ΔH ‡ = 8.1(3) kcal mol -1 and ΔS ‡ = -6.0(15) eu, which are broadly consistent with the calculated values. Calculations indicate that the exchange of phosphine donors at the boron center proceeds by an intrinsically dissociative mechanism. © 2011 The Royal Society of Chemistry.