Search results for "Isomerization"
showing 10 items of 281 documents
Anharmonic Vibrational Spectrum and Experimental Matrix Isolation Study of Thioformic Acid Conformers -- Potential Candidates for Molecular Cloud and…
2021
Thioformic acid (TFA) is the sulfur analog of formic acid, the simplest organic acid. It has three analogues HCOSH, HCSOH, and HCSSH, each of them having two rotational isomeric (rotameric) forms: trans and cis where the trans form is energetically more stable. In this article, we study computational energetics and anharmonic vibrational spectrum of TFA including overtone and combination vibrations. We also studied experimental photoisomerization and photodecomposition channels of HCOSH molecules with different wavelengths. We suggest that TFA is a potential sulfur containing candidate molecule for interstellar and planetary observations and discuss these in a light of different radiation e…
Photochemical behavior in azobenzene having acidic groups. Preparation of magnetic photoresponsive gels
2011
[EN] The photochemistry of three azobenzenes representing contrasting photochemical behaviors is described in the present work. Thus, Methyl Orange (MO, 4-[[(4-dimethylamino)phenyl]-azo]benzenesulfonic acid sodium salt, hereinafter (1) and 4-hydroxyazobenzene-4'-sulfonic acid (2) undergo in water fast photochemical proton shift, with decays in the microsecond timescale. In contrast to the previous cases, azobenzene-4,4'-dicarboxylic acid (3) undergoes photoisomerization in water. This photochemical behavior allows the preparation of aqueous gels with Aerosil as gelating agent (5% weight) exhibiting high cyclability and photoreversible isomerization of the trans to cis (300 nm irradiation) a…
Alkoxy substituted (E,E)-3,6-bis(styryl)pyridazine—a photosensitive mesogen for liquid crystals
2008
Abstract (E,E)-3,6-Bis(styryl)pyridazines (3a–t) bearing 2, 4 or 6 alkoxy chains were prepared by applying the Siegrist reaction of 3,6-dimethylpyridazine (13) and the corresponding azomethines 10a–t. The transversal dipole moment of these calamitic compounds effects an extremely high tendency for self-organization in thermotropic LC phases (N, SA, SB, SC, SE, SI/F, and Cub). The conjugated core structure represents moreover a chromophore with a high photosensitivity for (E,E)⇄(E,Z) isomerization reactions: this property makes the compounds interesting for optical imaging and switching techniques.
Computational evidence in favor of a two-state, two-mode model of the retinal chromophore photoisomerization
2000
In this paper we use ab initio multiconfigurational second-order perturbation theory to establish the intrinsic photoisomerization path model of retinal chromophores. This is accomplished by computing the ground state ( S 0 ) and the first two singlet excited-state ( S 1 , S 2 ) energies along the rigorously determined photoisomerization coordinate of the rhodopsin chromophore model 4- cis -γ-methylnona-2,4,6,8-tetraeniminium cation and the bacteriorhodopsin chromophore model all- trans -hepta-2,4,6-trieniminium cation in isolated conditions. The computed S 2 and S 1 energy profiles do not show any avoided crossing feature along the S 1 reaction path and maintain an energy gap >20 kcal⋅…
Trans-to-cis photoisomerization of cyclocurcumin in different environments rationalized by computational photochemistry
2020
International audience; Cyclocurcumin is a turmeric component that attracted much less attention compared to the well known curcumin. In spite of the less deep charcaterization of its properties, cyclocurcumin has shown promising anticancer effects when used in combination with curcumin. Especially, due to its peculiar molecular structure, cyclocurcumin can be regarded as an almost ideal photoswitch, whose capabilities can also be exploited for relevant biological applications. Here, by means of state-of-the-art computational methods for electronic excited-state calculations (TD-DFT, MS-CASPT2, XMS-CASPT2) we analyze in detail the absorption and photoisomerization pathways leading from the …
Ionization potential of Al6 and Al7 as a function of temperature
1999
The temperature-depence of the ionization potential of Al6 and Al7 clusters is studied by using ab initio molecular dynamics. The threshold regions of theoretical photoionization efficiency curves are obtained from the calculated ionization potential distributions by integration and the determined ionization potentials are compared with the experimental ones. Two important effects, which complicate the determination of ionization potential from photoionization efficiency curves, are observed: the thermal tail effect and the isomerization. Also a link between the adiabatic ionization potential and the threshold of the photoionization efficiency curve is discussed. In the case of Al7, this of…
Ionization potential of Al6 and A17 as a function of temperature
1999
The temperature-depence of the ionization potential of Al6 and Al7 clusters is studied by using ab initio molecular dynamics. The threshold regions of theoretical photoionization eciency curves are ob- tained from the calculated ionization potential distributions by integration and the determined ionization potentials are compared with the experimental ones. Two important eects, which complicate the determin- ation of ionization potential from photoionization eciency curves, are observed: the thermal tail eect and the isomerization. Also a link between the adiabatic ionization potential and the threshold of the photoion- ization eciency curve is discussed. In the case of Al7, this often use…
A NOT gate in a cis-trans photoisomerization model
2007
We numerically study the implementation of a NOT gate by laser pulses in a model molecular system presenting two electronic surfaces coupled by non adiabatic interactions. The two states of the bit are the fundamental states of the cis-trans isomers of the molecule. The gate is classical in the sense that it involves a one-qubit flip so that the encoding of the outputs is based on population analysis which does not take the phases into account. This gate can also be viewed as a double photo-switch process with the property that the same electric field controls the two isomerizations. As an example, we consider one-dimensional cuts in a model of the retinal in rhodopsin already proposed in t…
Manipulation of the ferroelectricity in LC polymers via photomechanical isomerization of azobenzene moieties
1996
We report the synthesis and characterization of a new ferroelectric liquid crystalline side chain copolymer containing photoisomerizable chromophores and non-photoisomerizable mesogenic units. On illumination with UV-light a suppression of the polar order is obtained as indicated by a substantial drop of the spontaneous polarization (Ps) compared to the dark state. We interpret this as the phase order being disrupted by the cis-isomer of the chromophore. After illumination with VIS-light only the major part of Ps is restored. The photochemical cis-trans back-isomerization (restoration of the phase) leads to a different stationary state than the dark state of the material. The thermal reisom…
On the anionic polymerization of dialkylaminoisoprenes, 3. A nuclear magnetic resonance study of the structure of oligo[5-(N,N-diisopropylamino)isopr…
1995
The structure of oligo[(5-N,N-diisopropylamino)isoprenyllithium] (number-average degree of polymerization Pn = 1-2) prepared by reaction of alkyllithium with 5-(N,N-diisopropylamino)-isoprene1 in nonpolar (benzene) and polar (tetrahydrofuran) solvents has been studied by 1H and 13C NMR spectroscopy. In tetrahydrofuran, as expected, the negative charge at the terminal chain unit is more delocalized than in benzene and, consequently, the carbon-lithium bond has a more ionic character. In both solvents the living chain end shows a cisoid-4, 1-structure. No cistrans isomerization could be detected. This independence of the carbanion structure of the solvent polarity is explained by the complexa…