Fluorescence of free complex molecules

A number of phenomena that determine the nature of the fluorescence of free complex molecules and the possibility of its analytical application are considered. Attention is specially paid to the specific features of the energetics of radiationless transitions, the role of statistical factors in the formation of spectral properties and the interrelationship among the luminescence-spectrum characteristics of rarefied vapors of complicated molecules, and the processes of energy transfer in collisions. The properties of polarized fluorescence of hot and jet-cooled vapors, the processes of relaxation of anisotropy in time and during collision reorientation, and transfer of anisotropy in photodisintegration are analyzed. Institute of Molecular and Atomic Physics, National Academy of Sciences of Belarus, 70, F. Skorina Ave., Minsk, 220072, Belarus. Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 65, No. 5, pp. 620–634, September–October, 1998.     

Circuit-Cocircuit Reversing Systems in Regular Matroids

We consider that two orientations of a regular matroid are equivalent if one can be obtained from the other by successive reorientations of positive circuits and/or positive cocircuits. We study the inductive deletion-contraction structure of these equivalence classes in the set of orientations, and we enumerate these classes as evaluations of the Tutte polynomial. This generalizes the results in digraphs from a previous paper. Received January 10, 2006     

Experimental determination of rotational motion correlation times of choline iodide in aqueous solutions

The influence of complexation on the molecular reorientation of choline iodide in dilute aqueous solutions was determined using the multiplet relaxation effect of ¹³C nuclei. __________ Published in Russian in Izvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 1111–1114, May, 2005.     

A Chemotactic Colloidal Motor

Chemotaxis plays a crucial role in the realization of various functions of human life such as fertilization, immune function, inflammatory response, regeneration processes, etc. Inspired by the natural chemotaxis, colloidal motors with chemotactic ability can realize intelligent sense and targeted navigation, which bring a revolutionary method to biomedical applications like precision medicine. However, the application in the biomedical field requires the colloidal motors with submicrometer scale, strong chemotactic ability and clear chemotactic mechanism. In this Concept article, we introduce the recent progress of chemotactic colloidal motors, covering the fundamental theory behind experimental advancements. Particularly, the torque-driven reorientation motion of the submicrometer-sized colloidal motors during chemotaxis is discussed, and also their underlying mechanism is proposed. With the continuous research on chemotactic colloidal motors, it is believed that the emerging chemotactic colloidal motors will broaden practical applications in the biomedical field.     

The effect of Er doping on the spin reorientation transition in Ho1−xErxAl2

The magnetothermal properties of pseudo binary Ho_1−xEr_xAl₂ alloys have been investigated by heat capacity measurements. Two anomalies are observed in the heat capacity of HoAl₂. A sharp peak at 20 K represents the first order spin reorientation transition, and a second order anomaly occurs in the vicinity of the ferromagnetic transition at 32 K. As Ho is partially replaced by Er in Ho_1−xEr_xAl₂ the sharpness of the first order heat capacity peak diminishes with increasing Er concentration, while the temperature of this transition remains practically unaffected. The second order ferromagnetic transition shifts to higher temperature region with increasing Er concentration. The observed behaviors are explained considering the geometry of 4f charge densities of Ho³⁺ and Er³⁺ and the easy magnetization directions of HoAl₂ and ErAl₂.     

Combination of molecular rods and half-discs: transition from lamellar to columnar order in multichain mononuclear ortho-palladated metallomesogens

Novel ortho-palladated phenylpyrimidine-1,3-diketonato organyls with successively increasing numbers of alkyl chains were synthesized and investigated by polarizing optical microscopy and X-ray diffraction. A discontinuous transition from a lamellar to a columnar organization is observed, dependent on the number of chains: molecules with four or five chains from smectic phases (SmA, SmC), the related compound with six chains in the molecule is nonmesomorphic, whereas molecules with seven or eight chains form hexagonal columnar mesophases.     

Multiferroic properties in terbium orthoferrite

Multiferroic properties in a polycrystalline terbium orthoferrite are investigated. Different thermomagnetic behaviors are observed in different magnetic fields, which is attributed to the suppression of the low temperature magnetic phase by an external magnetic field. Further studies reveal that the ferroelectricity originates from the spin configuration below3.5 K. In addition, the magnetic field control of electric polarization and dielectric constant is observed, which suggests a magnetoelectric effect in TbFeO3. The origin of ferroelectricity in this rare-earth orthoferrite is discussed.     

Influence of Curing Frequency on the Morphology and the Electro-Optical Property of Polymer-Stabilized Cholesteric Textures

The effect of curing frequency on the morphology of polymer networks and the electro-optical property of normal-mode polymer-stabilized cholesteric textures (PSCTs) has been investigated. The scanning electron microscopy indicates that the shape of polymer networks transforms from honeycomb-like to fiber-like due to the increased solubility of the monomer at higher curing frequencies. The PSCTs cured at lower frequencies with sufficiently large network voids show a two-stage reorientation process that correlates with two kinds of cholesteric liquid crystal (LC) under different environments. The threshold voltage decreases as the curing frequency increases from 1 Hz to 10,000 Hz, while the field-off response time increases.     

Investigations on liquid crystalline partially fluorinated alkyl and succinimidyl benzoates

The synthesis and mesophase properties of partially fluorinated alkoxy‐substituted benzoic alkyl and succinimidyl (NHS) esters with one, two and three perfluoroalkyl alkoxy chains are reported. The mesophases were studied using differential scanning calorimetry (DSC), polarizing optical microscopy and X‐ray diffraction of non‐oriented samples. The SmA phases of the one‐chain methyl esters are monotropic, while those of the one‐chain NHS esters are enantiotropic. The more wedge‐shaped two‐ and three‐chain alkyl esters do not form mesophases, whereas the succinimidyl analogues exhibit hexagonal columnar phases. Their enhanced mesophase stability is caused by the higher polarity of the succinimidyl ring with respect to the alkyl ester groups. Aggregation of the dipolar succinimidyl groups, together with the microsegregation of the lipophilic and fluorophilic segments of the partially fluorinated alkoxy chains, is assumed to lead to a threefold structured morphology in both the SmA and the Col_h phases. This threefold structuring can be regarded as analogous to known morphologies of ABC triblock copolymers.