1977
DOI: 10.1016/0009-2614(77)85317-7
|View full text |Cite
|
Sign up to set email alerts
|

Fluorescence from γ-irradiated solutions of naphthalene and naphthalene-d8. Effect of an applied magnetic field

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

2
2
0

Year Published

1979
1979
2015
2015

Publication Types

Select...
7

Relationship

0
7

Authors

Journals

citations
Cited by 10 publications
(4 citation statements)
references
References 11 publications
2
2
0
Order By: Relevance
“…2 and 3 is consistent with the theory (2, 3), and with our earlier results (6)(7)(8). The enhancement of the emission intensity increases with increasing magnetic field and approaches a plateau at fields > 0.1 T. The high field value varies with solvent in the order cyclohexane < squalane < isooctane for all solutes.…”
Section: Discussionsupporting
confidence: 91%
See 2 more Smart Citations
“…2 and 3 is consistent with the theory (2, 3), and with our earlier results (6)(7)(8). The enhancement of the emission intensity increases with increasing magnetic field and approaches a plateau at fields > 0.1 T. The high field value varies with solvent in the order cyclohexane < squalane < isooctane for all solutes.…”
Section: Discussionsupporting
confidence: 91%
“…Thus the rate of loss of spin correlation was calculated to be lower for deuterated compounds (2, 3), leading to a smaller magnetic field effect at high fields. This has been confirmed experimentally with naphthalene and naphthalene-d, (8). However, at low fields, the opposite effect was observed, i.e., the enhancement of the fluorescence intensity was higher for naphthalene-d, than for naphthalene.…”
supporting
confidence: 55%
See 1 more Smart Citation
“…fluorene, anthracene, naphthalene) in hydrocarbon solvents (e.g. squalane, cyclohexane) that form magnetically sensitive, geminate radical ion pairs upon illumination and which recombine to fluorescent excited states; [18][19][20][21][22][23] and photoexcited pyrene and N,N-dimethylaniline solutions for which spin-selective recombination results in a fluorescent exciplex. 17,24,25 An alternative two-colour approach, in which a second excitation source excites fluorescence in a reaction product, has been used to study the photochemistry of anthraquinone in micellar solutions.…”
Section: Introductionmentioning
confidence: 99%