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排序方式: 共有217条查询结果,搜索用时 46 毫秒
1.
JETP Letters - Analytical expressions have been obtained for the resonance component of the interlayer conductivity of quasi-two-dimensional conductors in an inclined magnetic field in the presence... 相似文献
2.
Yuliya Terentyeva Ye. Yu. Stepanenko A. M. Rashevska P. Yu. Koval 《Molecular Crystals and Liquid Crystals》2020,698(1):65-77
AbstractThe results of an experimental study of luminescence of an aqueous solution of adenosine triphosphate (ATP) at room temperature are presented. High-temperature fluorescence of low- and high-concentrated solution was experimentally detected and analyzed. The shape of the fluorescence spectrum, the excited state lifetime and the temperature behavior of the emission intensity indicate the formation in the high-concentrated solution of rather stable dimer-like complexes, which can form excimer states. 相似文献
3.
Zhu Wu Jrn Nitsch Julia Schuster Alexandra Friedrich Katharina Edkins Marcel Loebnitz Fabian Dinkelbach Vladimir Stepanenko Frank Würthner Christel M. Marian Lei Ji Todd B. Marder 《Angewandte Chemie (International ed. in English)》2020,59(39):17137-17144
Achieving highly efficient phosphorescence in purely organic luminophors at room temperature remains a major challenge due to slow intersystem crossing (ISC) rates in combination with effective non‐radiative processes in those systems. Most room temperature phosphorescent (RTP) organic materials have O‐ or N‐lone pairs leading to low lying (n, π*) and (π, π*) excited states which accelerate kisc through El‐Sayed's rule. Herein, we report the first persistent RTP with lifetimes up to 0.5 s from simple triarylboranes which have no lone pairs. RTP is only observed in the crystalline state and in highly doped PMMA films which are indicative of aggregation induced emission (AIE). Detailed crystal structure analysis suggested that intermolecular interactions are important for efficient RTP. Furthermore, photophysical studies of the isolated molecules in a frozen glass, in combination with DFT/MRCI calculations, show that (σ, B p)→(π, B p) transitions accelerate the ISC process. This work provides a new approach for the design of RTP materials without (n, π*) transitions. 相似文献
4.
Control over the Self‐Assembly Modes of PtII Complexes by Alkyl Chain Variation: From Slipped to Parallel π‐Stacks 下载免费PDF全文
Dr. Naveen Kumar Allampally Dr. María José Mayoral Dr. Sarayute Chansai Dr. María Cristina Lagunas Prof. Christopher Hardacre Dr. Vladimir Stepanenko Prof. Rodrigo Q. Albuquerque Prof. Dr. Gustavo Fernández 《Chemistry (Weinheim an der Bergstrasse, Germany)》2016,22(23):7810-7816
We report the self‐assembly of a new family of hydrophobic, bis(pyridyl) PtII complexes featuring an extended oligophenyleneethynylene‐derived π‐surface appended with six long (dodecyloxy ( 2 )) or short (methoxy ( 3 )) side groups. Complex 2 , containing dodecyloxy chains, forms fibrous assemblies with a slipped arrangement of the monomer units (dPt???Pt≈14 Å) in both nonpolar solvents and the solid state. Dispersion‐corrected PM6 calculations suggest that this organization is driven by cooperative π–π, C?H???Cl and π–Pt interactions, which is supported by EXAFS and 2D NMR spectroscopic analysis. In contrast, nearly parallel π‐stacks (dPt???Pt≈4.4 Å) stabilized by multiple π–π and C?H???Cl contacts are obtained in the crystalline state for 3 lacking long side chains, as shown by X‐ray analysis and PM6 calculations. Our results reveal not only the key role of alkyl chain length in controlling self‐assembly modes but also show the relevance of Pt‐bound chlorine ligands as new supramolecular synthons. 相似文献
5.
Dr. Vladimir Stepanenko Dr. Xue‐Qing Li Jana Gershberg Prof. Dr. Frank Würthner 《Chemistry (Weinheim an der Bergstrasse, Germany)》2013,19(13):4176-4183
The self‐assembly behavior of an achiral perylene bisimide (PBI) organogelator that bears two 3,4,5‐tridodecyloxybenzoylaminoethyl substituents at the imide positions has been investigated in chiral solvents (R)‐ and (S)‐limonene in great detail by circular dichroism (CD) spectroscopy and atomic force microscopy (AFM). CD spectroscopic studies on dilute solutions revealed a preferential population of one‐handed helical assemblies in chiral solvent with an enantiomeric excess close to 100 %, whereas AFM images of more than 100 nanofibers of the organogel obtained from more concentrated solutions were found to consist of both handed helices with an enantiomeric excess of only 20 %. This discrepancy is attributed to the fast gelation process at high dye concentration that evidently proceeds through non‐equilibrated nuclei in a kinetic rather than thermodynamic self‐assembly process. Under these conditions the chiral induction from the homochiral solvent may not be adequate in effectively populating only one‐handed helices. 相似文献
6.
The bulk of the analytical data of a long period was used for estimation of RSD values of the CHNS analysis results obtained by EuroVector EA-3000 in the single-reactor mode. It is shown that the accident error level is conducted with the sample preparation procedure as well as with the properties of the certain analyzed samples. It is established that the experimental obtained CHNS analysis error levels significantly differ from those given in the technical specifications. In case of analysis of sample with the unknown composition the accidental errors of determination of each element are comparable with the standard sample ones. 相似文献
7.
Markus Hecht Dr. Pawaret Leowanawat Tabea Gerlach Dr. Vladimir Stepanenko Dr. Matthias Stolte Prof. Dr. Matthias Lehmann Prof. Dr. Frank Würthner 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2020,132(39):17232-17238
A new perylene bisimide (PBI), with a fluorescence quantum yield up to unity, self-assembles into two polymorphic supramolecular polymers. This PBI bears four solubilizing acyloxy substituents at the bay positions and is unsubstituted at the imide position, thereby allowing hydrogen-bond-directed self-assembly in nonpolar solvents. The formation of the polymorphs is controlled by the cooling rate of hot monomer solutions. They show distinctive absorption profiles and morphologies and can be isolated in different polymorphic liquid-crystalline states. The interchromophoric arrangement causing the spectral features was elucidated, revealing the formation of columnar and lamellar phases, which are formed by either homo- or heterochiral self-assembly, respectively, of the atropoenantiomeric PBIs. Kinetic studies reveal a narcissistic self-sorting process upon fast cooling, and that the transformation into the heterochiral (racemic) sheetlike self-assemblies proceeds by dissociation via the monomeric state. 相似文献
8.
Dr. Christina Rest Dr. Divya Susan Philips Torsten Dünnebacke Dr. Papri Sutar Dr. Angel Sampedro Jörn Droste Dr. Vladimir Stepanenko Prof. Dr. Michael Ryan Hansen Dr. Rodrigo Q. Albuquerque Prof. Dr. Gustavo Fernández 《Chemistry (Weinheim an der Bergstrasse, Germany)》2020,26(44):10005-10013
Besides their widespread use in coordination chemistry, 2,2’-bipyridines are known for their ability to undergo cis–trans conformational changes in response to metal ions and acids, which has been primarily investigated at the molecular level. However, the exploitation of such conformational switching in self-assembly has remained unexplored. In this work, the use of 2,2’-bipyridines as acid-responsive conformational switches to tune supramolecular polymerization processes has been demonstrated. To achieve this goal, we have designed a bipyridine-based linear bolaamphiphile, 1 , that forms ordered supramolecular polymers in aqueous media through cooperative aromatic and hydrophobic interactions. Interestingly, addition of acid (TFA) induces the monoprotonation of the 2,2’-bipyridine moiety, leading to a switch in the molecular conformation from a linear (trans) to a V-shaped (cis) state. This increase in molecular distortion along with electrostatic repulsions of the positively charged bipyridine-H+ units attenuate the aggregation tendency and induce a transformation from long fibers to shorter thinner fibers. Our findings may contribute to opening up new directions in molecular switches and stimuli-responsive supramolecular materials. 相似文献
9.
The article presents novel design of non-contact rotary ultrasonic motor consisting of ring-shaped stator vibrating in in-plane flexural mode and rotor provided with blades. In contrast to other motors with similar design proposed motor relies on the use of standing ultrasonic waves. This simplifies design and electronic control of motor and becomes possible due to introduction of artificial asymmetry, for example by tilting one or several blades of the rotor relative to the surface normal. Operating principle of the proposed motor is based on acoustic radiation torque exerted on rotor by ultrasonic waves propagating in air or fluid gap between rotor and stator. This torque is calculated using finite element method by means of COMSOL Multiphysics software. Dynamics of rotor is studied using MathCad software and general theory of nonlinear conservative oscillators. Role of asymmetry is explained on the basis of comparative analysis of potential functions and phase trajectories for symmetric and asymmetric cases. It is shown that direction of rotation is determined by structural parameters of motor, particularly tilting direction (clockwise or counter-clockwise) of the blades. Conceptual design of motor with bidirectional rotation is described. Direction and velocity of rotation in the proposed conceptual design can be potentially controlled by changing excitation frequency of stator. 相似文献
10.
O. B. Maksimov R. P. Gorshkova L. S. Stepanenko N. P. Mishchenko O. E. Krivoshchekova 《Chemistry of Natural Compounds》1990,26(3):333-334
Pacific Ocean Institute of Bioorganic Chemistry, Far Eastern Branch, USSR Academy of Sciences, Vladivostok. Translated from
Khimiya Prirodnykh Soedinenii, No. 3, pp. 400–401, May–June, 1990. 相似文献