Transient ESR spectra have been observed for the lowest triplet states of naphthalene, quinoline (QN), quinolinium (QNH+), isoquinoline (iso-QN) and isoquinolinium (iso-QNH+) in ethanol at 77 K using a time-resolved ESR technique. With the aid of computer simulations, it is concluded that, following
A time-resolved electron spin resonance study of the triplet states of 2,2′-bipyridine and its singly protonated cation
✍ Scribed by Mikio Yagi; Yasuaki Deguchi; Yasushi Shioya; Jiro Higuchi
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- English
- Weight
- 368 KB
- Volume
- 144
- Category
- Article
- ISSN
- 0009-2614
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✦ Synopsis
Time-resolved ESR spectra have been observed for the lowest triplet states of 2,2'-bipyridine (bpy) and singly protonated bpy (bpyH+) in ethanol at 77 K. With the aid of computer simulation, it is concluded that the T, sublevel is most active in S, +T, intersystem crossing in both molecules studied and (P,-P,)l(P,-P,) changes from 9 in s-trans-bpy to 1.5 in bpyH+ (P, are relative populating rates; y and z, close to in-plane long and short axes, respectively).
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Time-resolved EPR spectra have been observed for the lowest triplet states of biphenyl, 4-phenylpyridine (PPY) and Cphenylpyridinium (PPYH+ ) in ethanol at 77 K The sublevel preferentially populated by intersystem crossing is T, (top sublevel) in biphenyl. Following the protonation of PPY, (P,,) /(
Time-resolved ESR spectra have been observed for the lowest excited triplet states of 1-nitronaphthalene and 1,4dinitronaphthalene in EPA at 77 K. The results show that the sublevel preferentially populated by intersystem crossing is T,, in both molecules studied (y is close to the in-plane long axi