Search results for "Chromis"
showing 10 items of 172 documents
Control of the thermal reaction of a photochromic spirobenzopyran by the enzyme-like activity of albumins
1997
Abstract The thermal ring-opening reaction of a negative photochronic spirobenzopyran was investigated in the presence and absence of albumins. In the presence of the proteins, the formation of the merocyanine form from the spiro form is enhanced markedly by two orders of magnitude. The results for five different albumins indicate the enzyme-like activity of the proteins. The influence of pH, temperature and various ligands was examined in detail for bovine serum albumin (BSA) and human serum albumin (HSA). In particular, it was deduced that warfarin shows reversible purely competitive inhibition for BSA with an inhibitor constant K 1 of 1.6×10 −3 M. The results suggest that the catalytic c…
Hybrid Molecular Materials Based upon the Photochromic Nitroprusside Complex, [Fe(CN)5NO]2-, and Organic π-Electron Donors. Synthesis, Structure, and…
2000
An organic/inorganic hybrid salt is obtained by combination of the photochromic nitroprusside complex with the organic donor TTF. The organic part shows an unprecedented 2D organization formed by an orthogonal arrangement of TTF hexamers and monomers. However, the donor layers are formed by pairs of moderately interacting dimeric (TTF)22+ units surrounded by neutral TTF molecules in such a way that the charge is localized and the compound is a semiconductor. Short contacts between the organic layers and the nitroprusside anions are present that may affect the photophysical properties of the nitroprusside.
Generalized synthesis of periodic surfactant/inorganic composite materials
1994
THE recent synthesis of silica-based mesoporous materials1,2 by the cooperative assembly of periodic inorganic and surfactant-based structures has attracted great interest because it extends the range of molecular-sieve materials into the very-large-pore regime. If the synthetic approach can be generalized to transition-metal oxide mesostructures, the resulting nanocomposite materials might find applications in electrochromic or solid-electrolyte devices3,4, as high-surface-area redox catalysts5 and as substrates for biochemical separations. We have proposed recently6 that the matching of charge density at the surfactant/inorganic interfaces governs the assembly process; such co-organizatio…
Probing the Folding of Peptide–Polymer Conjugates Using the π-Dimerization of Viologen End-Groups
2020
The synthesis of a foldable viologen-functionalized peptide–polymer conjugate is presented. The ABA-type triblock conjugate with a PEG polymer was capped with a FHFHF pentapeptide sequence and further modified with a viologen building block at both chain ends. The pH-responsive peptide domains fold into an intermediate structure inducing close proximity of the viologen units, which upon a reduction step form π-dimers of the radical cation. Overall the intramolecular folding and intermolecular self-assembly process leads to the formation of supramolecular nanorods. Mixing of viologen-peptide–polymer conjugates with unfunctionalized conjugates leads to crosslinking of the nanorods and hydroge…
<title>Cerium-containing counter electrodes for transparent electrochromic devices</title>
1997
Films of Me-Ce oxide (Me: Ti, Zr, Sn, W) and of Ni-Ce hydroxide were produced by reactive magnetron co-sputtering. Li intercalation in Me-Ce oxide, and H exchange in Ni-Ce hydroxide, were accomplished electrochemically. Electrochromism was quenched in proportion with the Ce content in Me-Ce oxide. Films of Zr-Ce (and to some extent Ti-Ce) oxide were able to serve as fully transparent counter electrodes, of much interest for transparent electrochromic devices. In Ni-Ce hydroxide, the Ce addition enhanced the capacity for charge exchange.
Tristriazolotriazines with π-Conjugated Segments: Star-Shaped Fluorophors and Discotic Liquid Crystals
2012
C3-symmetrical tristriazolotriazines substituted with phenylene rings carrying lateral flexible alkoxy side chains were prepared via condensation/ring transformation of cyanuric chloride and tetrazoles. These star-shaped, planar compounds can form broad thermotropic mesophases. Due to the extensive π-conjugation, these compounds are highly emissive and the octupolar donor-acceptor electronic structure results in non-linear optical properties like solvatochromism. Brønstedt acids provoke halochromism of the absorption and of the fluorescence.
Macrocycles as Molecular Units to Build up Electroresponsive Materials: A Comparative Theoretical Investigation of the Electronic and Optical Propert…
1990
Besides their classical and well-known applications as, e.g., dyes, pigments, catalysts, etc. [1], phthalocyanines (Pc’s) have been of particular interest in many fields of basic and applied research concerning solar cells [2], photosensitizers [3], low dimensional metals [4], gas sensors [5], electrochromism [6], Langmuir-Blodgett (LB) films [7], and nonlinear optics [8]. As an example, gas sensors [9], electronic devices [10], laser recording materials [11], and photovoltaic cells [12] can now be built from LB films of phthalocyanines. This great variety of interesting applications results from a number of unique properties that phthalocyanines exhibit On the one hand, they show an except…
Light Induced Modifications of Langmuir-Blodgett-Multilayer Assemblies Containing Amphotropic Azocopolymer
1994
Abstract Photochromic LB-multilayers of amphotropic copolymers having rod-like azobenzene moieties as side groups which exhibit thermotropic liquid crystalline behaviour in the bulk have been characterized by UV-VIS spectroscopy as well as by angular dependent and energy dispersive SAXS. Upon irradiation with UV-light the initial optical in-plane anisotropy and the vertical layered structure of LB-films can be destroyed. A new layered structure can be rebuilt on irradiation with visible light or by annealing. Using linearly polarized light for the irradiation an optical anisotropy (POA) has been induced or reversibly modified by a photoselection process.
ChemInform Abstract: Diaryldistyrylpyrazines: Solvatochromic and Acidochromic Fluorophores.
2014
Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photophysics is controlled by the styryl substitution, the diaryl substituents on the central pyrazine only having a small effect. Protonation occurs on the pyrazine and/or lateral amines or azines, thereby altering the absorption and emission properties. Hypso- and bathochromism as well as fluorescence quenching depend on the nature of the terminal substituent. This, and a significant positive solvatochromism of the fluorescence, allow optical sensing of t…
Diaryldistyrylpyrazines: Solvatochromic and Acidochromic Fluorophores
2013
Diaryldimethylpyrazines are the starting materials for the synthesis of C2-symmetric donor- or acceptor-substituted distyrylpyrazines. The optical properties of these cruciform-shaped dyes are dominated by the distyrylpyrazine units; the photophysics is controlled by the styryl substitution, the diaryl substituents on the central pyrazine only having a small effect. Protonation occurs on the pyrazine and/or lateral amines or azines, thereby altering the absorption and emission properties. Hypso- and bathochromism as well as fluorescence quenching depend on the nature of the terminal substituent. This, and a significant positive solvatochromism of the fluorescence, allow optical sensing of t…