1979
DOI: 10.1063/1.438845
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Erratum: Fluorescence transient and optical free induction decay spectroscopy of pentacene in mixed crystals at 2 K. Determination of intersystem crossing and internal conversion rates [J. Chem. Phys. 70, 5807 (1979)]

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Cited by 45 publications
(72 citation statements)
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“…M TCþ , via decreasing concen tration), the size of this jump diverges. Our model predicts that the This result of our rigorous theory complements the simple geometric diffuse cone argument of de Vries [14], which is shown in Figure 6. The conventional, but oversimplified, relationship between layer contraction and tilt angle, D d ¼ (1 � cos(h)), is obtained geometri cally by assuming a liquid crystal with perfect orientational order, as shown in Figure 6(a).…”
supporting
confidence: 53%
“…M TCþ , via decreasing concen tration), the size of this jump diverges. Our model predicts that the This result of our rigorous theory complements the simple geometric diffuse cone argument of de Vries [14], which is shown in Figure 6. The conventional, but oversimplified, relationship between layer contraction and tilt angle, D d ¼ (1 � cos(h)), is obtained geometri cally by assuming a liquid crystal with perfect orientational order, as shown in Figure 6(a).…”
supporting
confidence: 53%
“…When embedded in p-terphenyl at liquid-helium temperatures, the O 3 and O 4 sites have rates exceeding those of the O 1 and O 2 sites by two orders of magnitude. 12,13 When increasing the temperature, the O 1 and O 2 ISC rates were observed to converge to those of O 3 and O 4 . 13,14 For pentacene in benzoic acid at 1.6 K, the ISC was shown to be dominated by a near-resonance of the first excited singlet state S 1 and a vibrational level of a higher triplet state.…”
Section: Introductionmentioning
confidence: 99%
“…Normally, the layers contract below the transition from SmA* -where θ ≡ 0 in absence of fields -to SmC* or one of its AFLC variations. In some compounds this shrinkage is much smaller than expected, a behaviour which was explained by the Dutch-American crystallographer Adriaan de Vries. He recognised that one must take into account that the molecules have a non-zero average inclination θ mol away from k even if θ = 0, as in SmA*, a result of the orientational disorder characteristic of any LC phase [16][17][18][19]. The uniaxial symmetry around k and the absence of director tilt are consequences of the fact that all directions of molecule inclination are equally probable in the orientational fluctuations.…”
Section: Introductionmentioning
confidence: 99%