A new transient absorption spectrum observed in the flash photolysis of thiophene

1978 ◽  
Vol 55 (1) ◽  
pp. 116-118 ◽  
Author(s):  
S.L.N.G. Krishnamachari ◽  
T.V. Venkitachalam
1992 ◽  
Vol 47 (12) ◽  
pp. 1243-1247 ◽  
Author(s):  
I. Timtcheva ◽  
N. Getoff ◽  
P. Nikolov ◽  
R. M. Quint

Steady state as well as flash photolysis experiments of 2-aryl-3-imino-1-indones (2-AIID) have been carried out with the aim to learn more about their photochemical properties. It was established that in ethanol these substances exist solely in the keto-enamine-form and are rather photostable under the influence of uv-light. Illumination in dichloroethane, acetonitrile and dioxane is leading to stable photoproducts. A typical transient absorption spectrum of 2-AIID is presented. Probable reaction mechanisms are given.


1965 ◽  
Vol 43 (10) ◽  
pp. 1795-1830 ◽  
Author(s):  
A. J. Merer ◽  
D.N. Travis

A new transient absorption spectrum, attributed to the CCN free radical, has been discovered in the flash photolysis of diazoacetonitrile, HC(CN)N2; three electronic transitions, between 3 500 Å and 4 700 Å, have been photographed for both CC14N and CC15N. The ground state of the radical is a 2Πr electronic state, and the three excited states observed are A2Δ, B2Σ−, and C2Σ+. The 2Π and 2Δ states show evidence of Renner–Teller interaction between the vibrational and electronic angular momenta, an effect not observed previously for 2Δ states. Theoretical expressions for the vibrational energy levels of linear triatomic molecules in 2Δ electronic states have been derived, in terms of a parameter η associated with the quartic terms in the potential energy. They are compared with the observed pattern in the ν2 = 1 level of the A2Δ state. The principal molecular constants for CC14N (in cm−1) are as follows:[Formula: see text]


2003 ◽  
Vol 0 (7) ◽  
pp. 2606-2609
Author(s):  
M.-S. Nomura ◽  
M. Arita ◽  
S. Ashihara ◽  
S. Kako ◽  
M. Nishioka ◽  
...  

2018 ◽  
Vol 97 (3) ◽  
Author(s):  
Andrew Chew ◽  
Nicolas Douguet ◽  
Coleman Cariker ◽  
Jie Li ◽  
Eva Lindroth ◽  
...  

2007 ◽  
Vol 11 (05) ◽  
pp. 368-374 ◽  
Author(s):  
Shunichi Fukuzumi ◽  
Yukiyasu Kashiwagi

A supramolecular ferrocene-zinc porphyrin-pyridylnaphthalenediimide triad is formed by coordinating the pyridine entity of pyridylnaphthalenediimide with the zinc ion of a ferrocene-zinc porphyrin dyad in benzonitrile. The fluorescence of the zinc porphyrin moiety is efficiently quenched by photoinduced electron transfer from the singlet excited state of the zinc porphyrin moiety to the naphthalenediimide moiety. This is followed by subsequent electron transfer from the ferrocene moiety to the zinc porphyrin radical cation to produce the final charge-separated state, ferricenium ion-zinc porphyrin-naphthalenediimide radical anion, which is successfully detected as a transient absorption spectrum in the laser flash photolysis. The decay of the charge-separated state obeys first-order kinetics irrespective of the initial concentration of the charge-separated state to afford a long lifetime (320 μs). This is the first example of a supramolecular triad that has a long lifetime as compared with the charge-separated state lifetime of the component dyad.


1966 ◽  
Vol 44 (7) ◽  
pp. 1541-1550 ◽  
Author(s):  
A. J. Merer ◽  
D. N. Travis

A new transient absorption spectrum, belonging to the HCF free radical, has been discovered in the flash photolysis of dibromofluoromethane, HCFBr2. The spectrum consists of a single progression of complex bands in the region 4 300–6 000 Å. Rotational analysis of the less severely perturbed bands shows them to be type-C bands of a molecule that is nonlinear in both upper and lower states of the transition, with bond angles of ~ 127° and ~ 102° respectively. Axis-switching effects, due to the large change of bond angle in the transition, cause the appearance of prominent gQ, qQ, and °Q branches, in addition to those obeying the ordinary type-C selection rules.The principal molecular constants of HCF (in cm−1) are:[Formula: see text]


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