Photochromism of spiroindolinonaphthoxazine. I. Photophysical properties

1983 ◽  
Vol 61 (2) ◽  
pp. 300-305 ◽  
Author(s):  
Nori Y. C. Chu

A solution of spiroindolinonaphthoxazine in a common organic solvent shows profound photochromic effect. The colorless form in ethanol displays three absorption bands (~320, 235, 203 nm) in the ultraviolet region of the spectrum. The absorption spectrum of the colored metastable form shows two prominent absorption peaks at 612 and 578 nm. The triplet state energy level of the colorless form is estimated to be in the range from 2.4 × 104 to 2.1 × 104 cm−1 by the triplet–triplet energy transfer method. There exists a thermal equilibrium between the colorless and colored forms. From the measurement of absorbance of the colored form at different temperatures, the standard enthalpy of equilibrium is obtained (ΔH0 = 1500 cm−1). The thermal decay of the colored form to the colorless form depends strongly on temperature. The decay rate increases three times for every 10 °C increase in temperature. From these temperature dependence studies of the thermal decay rate, the thermal energy barrier for the colored metastable state to decay to the colorless form is determined to be 6.9 × 103 cm−1.

2002 ◽  
Vol 725 ◽  
Author(s):  
Seiichi Furumi ◽  
Akira Otomo ◽  
Shiyoshi Yokoyama ◽  
Shinro Mashiko

AbstractThis report describes the synthesis of photocrosslinkable dendrimers with peripheral cinnamamide residues, which exhibit both photoisomerization and photodimerization, and their photochemical and photophysical properties in dilute solutions and polymer matrices. Photoirradiation with 313 nm gave rise to monotonous decrease in the absorbance of trans-cinnamamide at 270 nm as a result of the photochemical reactions of the cinnamamide residues. Spectral analysis revealed the changes in the photoproduct distribution of trans- and cis-photoisomerized and photodimerized cinnamamide groups to be a function of the exposure energy. In dilute solutions, the first-generation dendrimer displayed preferential formation of cis-isomer of the cinnamamide, whereas the photodimerization took place more favorably for the third- and fifth-generation dendrimers. The photochemical behavior was strongly dependent on the dendrimer generation rather than the concentration, probably due to the extent of steric crowding among the cinnamamide residues at terminal positions. Furthermore, the third- and fifth-generation dendrimers showed capturability of a benzophenone derivative into the macromolecules and triplet-triplet energy transfer in the photocrosslinkable dendrimers. This novel phenomenon of the triplet-triplet energy transfer in the dendritic cavities suggests potential applicability to design and fabricate novel optical and electrical molecular devices.


2006 ◽  
Vol 10 (08) ◽  
pp. 1049-1060 ◽  
Author(s):  
Prashanth Kumar Poddutoori ◽  
Premaladha Poddutoori ◽  
Bhaskar G. Maiya

A bis(terpyridine)ruthenium(II) complex ([Ru]2+) was covalently connected via a floppy - OCH 2 CH 2 O - spacer to the free-base porphyrin (H) or zinc(II) porphyrin (Zn) or both, to obtain dyads ([HRu]2+, [ZnRu]2+) and triads ([HRuH]2+, [ZnRuH]2+, [ZnRuZn]2+). These compounds have been fully characterized by MALDI, UV-vis, 1 H NMR (1D and 1 H -1 H COSY) spectroscopies, and also by the cyclic and differential pulse voltammetric techniques. Absorption spectroscopy of these newly synthesized compounds shows that significant exciton coupling exists in non-polar solvents (cyclohexane and toluene) between the porphyrin ring and the bis(terpyridine)ruthenium(II) complex. Upon excitation within the Soret band of [HRu]2+/[HRuH]2+, free-base porphyrin fluorescence was found to be strongly quenched in non-polar and weakly quenched in polar solvents, probably due to ‘singlet-triplet’ energy transfer from the free-base porphyrin to the [Ru]2+ complex. Whereas, in [ZnRu]2+/[ZnRuZn]2+, zinc(II) porphyrin fluorescence was quantitatively and reasonably quenched in non-polar and polar solvents, respectively by mainly electron transfer from the zinc(II) porphyrin to the [Ru]2+ complex. The solvent plays a crucial role in the photophysical properties of these compounds, since the energy of the triplet metal-to-ligand charge-transfer (3MLCT) excited state is influenced by the polarity of the medium. Finally, [ZnRuH]2+ exhibits the combined fluorescence properties of [HRu]2+ and [ZnRu]2+ but the observed additional quenching in non-polar solvents for the zinc(II) porphyrin component is explained by energy transfer from the zinc(II) porphyrin to the free-base porphyrin and/or the bis(terpyridine)ruthenium(II) complex.


2020 ◽  
Author(s):  
Mauricio Lineros-Rosa ◽  
Antonio Francés-Monerris ◽  
Antonio Monari ◽  
Miguel Angél Miranda ◽  
Virginie Lhiaubet-Vallet

Interaction of nucleic acids with light is a scientific question of paramount relevance not only in the understanding of life functioning and evolution, but also in the insurgence of diseases such as malignant skin cancer and in the development of biomarkers and novel light-assisted therapeutic tools. This work shows that the UVA portion of sunlight, not absorbed by canonical DNA nucleobases, can be absorbed by 5-formyluracil (ForU) and 5-formylcytosine (ForC), two ubiquitous oxidative lesions and epigenetic intermediates present in living beings in natural conditions. We measure the strong propensity of these molecules to populate triplet excited states able to transfer the excitation energy to thymine-thymine dyads, inducing the formation of the highly toxic and mutagenic cyclobutane pyrimidine dimers (CPDs). By using steady-state and transient absorption spectroscopy, NMR, HPLC, and theoretical calculations, we quantify the differences in the triplet-triplet energy transfer mediated by ForU and ForC, revealing that the former is much more efficient in delivering the excitation energy and producing the CPD photoproduct. Although significantly slower than ForU, ForC is also able to harm DNA nucleobases and therefore this process has to be taken into account as a viable photosensitization mechanism. The present findings evidence a rich photochemistry crucial to understand DNA photodamage and of potential use in the development of biomarkers and non-conventional photodynamic therapy agents.


Author(s):  
Yi-Mei Huang ◽  
Tse-Ying Chen ◽  
Deng-Gao Chen ◽  
Hsuan-Chi Liang ◽  
Cheng-Ham Wu ◽  
...  

35Cbz4BzCN, a novel universal host with long triplet lifetime, has been developed. The triplet excitons in 35Cbz4BzCN can be effectively harvested by phosphorescence and thermally activated delayed fluorescence emitters. In...


2008 ◽  
Vol 78 (4) ◽  
Author(s):  
Ivan I. Fishchuk ◽  
Andrey Kadashchuk ◽  
Lekshmi Sudha Devi ◽  
Paul Heremans ◽  
Heinz Bässler ◽  
...  

2007 ◽  
Vol 111 (43) ◽  
pp. 10928-10937 ◽  
Author(s):  
Galina V. Loukova ◽  
Svetlana E. Starodubova ◽  
Vyatcheslav A. Smirnov

2014 ◽  
Vol 90 (3) ◽  
pp. 511-516 ◽  
Author(s):  
Azusa Kikuchi ◽  
Nozomi Oguchi-Fujiyama ◽  
Kazuyuki Miyazawa ◽  
Mikio Yagi

Sign in / Sign up

Export Citation Format

Share Document