Absolute stereochemistry of dihydrofuroangelicins bearing C-8 substituted double bonds: a combined chemical/exciton chirality protocolElectronic supplementary information (ESI) available: Relative energies and relevant geometrical parameters of DFT-optimized structures of sty-2 and sty-5 (Table ESI1). Calculated and experimental 3JMe8,H9a and 3JMe8,H9b values (in Hz) for sty-2 and sty-5 (Table ESI2). UV absorption spectrum of 7-hydroxy-4-methylcoumarin in CH3CN (Fig. ESI1). Description of the procedure for estimating transition dipole moment positions from excited-states calculations. See http://www.rsc.org/suppdata/ob/b3/b312542d/

2004 ◽  
Vol 2 (1) ◽  
pp. 48 ◽  
Author(s):  
Katsunori Tanaka ◽  
Gennaro Pescitelli ◽  
Lorenzo Di Bari ◽  
Tom L. Xiao ◽  
Koji Nakanishi ◽  
...  
Keyword(s):  
Absorption Spectrum ◽  
Dipole Moment ◽  
Excited States ◽  
Transition Dipole Moment ◽  
Uv Absorption ◽  
Supplementary Information ◽  
Geometrical Parameters ◽  
Transition Dipole ◽  
Absolute Stereochemistry ◽  
Uv Absorption Spectrum

Aza-substitution effect on the Q-band excitations of free-base porphin, chlorin, and bacteriochlorin: SAC-CI theoretical study

2005 ◽  
Vol 09 (05) ◽  
pp. 305-315 ◽  
Author(s):  
Jun-ya Hasegawa ◽  
Takayuki Kimura ◽  
Hiroshi Nakatsuji
Keyword(s):  
Dipole Moment ◽  
Excited States ◽  
Molecular Design ◽  
Decomposition Analysis ◽  
Substitution Effect ◽  
Transition Dipole Moment ◽  
Orbital Energy ◽  
Free Base ◽  
Transition Dipole ◽  
Near Degeneracy

Electronic structure of the excited states and absorption spectra of free-base azaporphins, azachlorin, and azabacteriochlorin were systematically investigated by SAC-CI calculations. Aza-substitution at the meso position affects the orbital energy of the next-HOMO, and the transition dipole moment enlarges as the number of the substitution increases. Some of the aza-substitutions dramatically affect the direction of the transition dipole, due to reduction of the molecular symmetry, which was studied in detail by a decomposition analysis of the transition dipole moment. Tetraza-substitution in chlorin and bacteriochlorin increases the oscillator strength more than that of tetrazaporphin. The mechanism underlying these changes originates mainly from the relaxation of near-degeneracy in the main configurations. These findings would be useful for the application to the molecular design of the excited states.

Multireference calculations of potential energy and transition dipole moment surfaces for first and second UV absorption bands of N2O

2014 ◽  
Vol 13 (02) ◽  
pp. 1450020
Author(s):  
Mohammad Noh Daud
Keyword(s):  
Dipole Moment ◽  
Potential Energy ◽  
Excited States ◽  
Transition Dipole Moment ◽  
Basis Set ◽  
Conical Intersections ◽  
Excitation Energies ◽  
Absorption Bands ◽  
Transition Dipole ◽  
Vertical Excitation

A great deal of theoretical work has been carried out to investigate the properties of the six lowest singlet electronic states of N 2 O molecule: the ground state X 1A′; the excited states 11A′′, 21A′, 21A′′, 31A′ and 31A′′. Multireference configuration interaction (MRCI) approach has been used to compute the full-dimensional potential energy surfaces of the six lowest states employing aug-cc-pVQZ minus g orbital basis set. It was found that such of highly accurate potential yields excellent results of bond dissociation and vertical excitation energies in comparison with the experimental values. Several important symmetry and nonsymmetry related conical intersections in linear and bent geometries have been discussed. Of particular interest is the location of conical intersections between the 21A′(1Δ) and 31A′(1Π) states, and between the 11A′′(1Σ-) and 31A′′(1Π) states in linear geometry, as well as conical intersection between the X 1A′ and 21A′ states in bent geometry. The corresponding transition dipole moment surfaces have also been computed, connecting the ground electronic state to the lowest five excited states. Detailed discussion on the vector properties of the dipole transition has been presented specifically in the vicinity of the conical intersections.

Theoretical studies on the one- and two-photon absorption of tetrabenzoporphyrins and phthalocyanines

2004 ◽  
Vol 82 (1) ◽  
pp. 19-26 ◽  
Author(s):  
Xin Zhou ◽  
Ai-Min Ren ◽  
Ji-Kang Feng ◽  
Xiao-Juan Liu
Keyword(s):  
Dipole Moment ◽  
Cross Sections ◽  
Density Functional ◽  
Transition Dipole Moment ◽  
Photon Absorption ◽  
Transition Dipole ◽  
Two Photon Absorption ◽  
Two Photon ◽  
Order Of Magnitude ◽  
The One

The one-photon absorption (OPA) properties of tetrabenzoporphyrins (TBPs) and phthalocyanines (Pcs) were studied using the semiempirical ZINDO method and time-dependent density functional theory (TDDFT), respectively. The compared results confirmed that the semiempirical ZINDO method was reasonably reliable when calculating the OPA of tetrabenzoporphyrins and phthalocyanines. On the basis of the OPA properties obtained from the ZINDO method, two-photon absorption (TPA) properties of two series of molecules were investigated, using ZINDO and sum-over-states (SOS) methods. The results showed that the TPA cross-sections of all molecules were in the range of 220.6 × 10–50 – 345.9 × 10–50 cm4·s·photon–1, which were in the same order of magnitude as the values reported in the literature. The relatively larger δ(ω) value for Pcs with respect to that for corresponding TBPs originates from larger intramolecular charge transfer, which can be characterized by the difference of dipole moment between S0 and S1 and the transition dipole moment between S1 and S5.Key words: two-photon absorption, ZINDO, sum-over-states, tetrabenzoporphyrin, phthalocyanines.

Lifetimes and transition dipole moment functions of NaK low lying singlet states: Empirical and ab initio approach

1998 ◽  
Vol 109 (16) ◽  
pp. 6725-6735 ◽  
Author(s):  
M. Tamanis ◽  
M. Auzinsh ◽  
I. Klincare ◽  
O. Nikolayeva ◽  
R. Ferber ◽  
...  
Keyword(s):  
Dipole Moment ◽  
Ab Initio ◽  
Transition Dipole Moment ◽  
Transition Dipole ◽  
Singlet States ◽  
Moment Functions ◽  
Ab Initio Approach

Fundamental Absorption Band of HD

1974 ◽  
Vol 52 (17) ◽  
pp. 1669-1671 ◽  
Author(s):  
J. Bejar ◽  
H. P. Gush
Keyword(s):  
Dipole Moment ◽  
Absorption Band ◽  
Line Width ◽  
Doppler Effect ◽  
Transition Dipole Moment ◽  
Vibration Band ◽  
Transition Dipole ◽  
Fundamental Absorption Band ◽  
The Doppler Effect

The fundamental rotation–vibration band of HD has been resolved in the gas at 1 atm pressure. The line width appears to be totally due to the Doppler effect and equals 0.026 cm−1. The transition dipole moment has been calculated from the intensities of lines in the R branch: it is found to vary from 4 × 10−5 D for J = 0 to 7 × 10−5 for J = 4.

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