A reinvestigation is reported of UV-laser-induced transient dielectric losses at microwave frequencies in solutions of 4-N,N-dimethylaminobenonitrile (DMABN) and related compounds in cyclohexane and 1,klioxane and of 9,9'-bianthryl in n-hexane. Excitation of DMABN and related compounds in cyclohexan
Dipole moments of singlet and triplet excited states of 4-N,N-dimethylaminobenzonitrile and related compounds and of their solute—solvent exciplexes
✍ Scribed by Robert J. Visser; Petra C.M. Weisenborn; Cyril A.G.O. Varma; Mathijs P. De Haas; John M. Warman
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- English
- Weight
- 803 KB
- Volume
- 104
- Category
- Article
- ISSN
- 0009-2614
No coin nor oath required. For personal study only.
✦ Synopsis
Changes in dielectric loss at microwave frequencies resulting from UV laser excitation of solutions of 4-N,N-dimethyfaminobsnzonitrile and some of its derivatives in cyclohexane and in lfl-dioxane have been studied. The changes are due to differences between the dipole moments of the sohste in the ground and excited states. ExcipIex formation with 1,4dioxane leads to a reduction of the excited-state dipole moment both where the amino group is restricted to be copIanar and where it is non-coplanar with the aromatic ring of the solute. We did not fmd indications of Iarge moIecuIar polarizabilities of DiMABN which could govern its ffuoresccnce behaviour and we have to reject the suggestion (TICf theory) that twisting of the amino group causes a Iarge increase of the dipole moment of DMABN in the Sr state.
📜 SIMILAR VOLUMES
TIP= relat.ivo salvation of the ground and the excited states corresponding to the n -L R\* W transition of carbonyl chromophores is determined, for a serie of solvents, on the basis of (11 the value of AE = hv, (2) the salvation enthaipy of the ground state determined by calorimetry, (3) the enthai