Nonadiabatic corrections to the dipole moments of HCI and DQ 318 calculntcd. Kaiser's deduction that the effect of the brmkdown of the Born-Oppenheimer approximation is to reduce the dipole of DC1 relative to iIQ by about 10S3 D is shown to b2 ialistic.
Evidence for the contribution of the lone pair to the molecular dipole moment of triarylphosphines
β Scribed by Mark P. Warchol; E.N. DiCarlo; Cynthia A. Maryanoff; Kurt Mislow
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- French
- Weight
- 219 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
We wish to report evidence that the overall dipole moment of triphenylphosphine and derivatives is dominated by the contribution of the partial moment of the lone pair on phosphorus. some phosphine years ago, the observation that the dipole moment (u) of trimesityl-(9, 1.37 D, is close to the range of moments (1.39 -1.54 D) report, 'I ed for triphenylphosphine (3 led us to the conclusionL that the C-P-C bond angles (9) in the former should not deviate much from those in the latter.
Our confident expectation that 1 should have bond angles near 103" was there-
π SIMILAR VOLUMES
Despite its antiparallel symmetry, DNA often appears to possess a permanent electric dipole moment in transient electro-optical experiments. We propose that this may be due to the asymmetric binding of charged ligands to the DNA. We have used the fluctuating dipole theory of Kirkwood and Shumaker to