Publications by authors named "Subbarao Krishna Prasad"

In the field of modern nanoscience, the ability to tailor the properties of nanoparticles is essential for advancing their applications. A key approach for achieving this control involves manipulating surface plasmon resonance (SPR) to modify optical properties. This study introduces a novel method for synthesizing gold nanoparticles capped with photoactive liquid crystalline azo ligands, accomplished without reducing agents.

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Polymers reinforced with nanofillers, especially graphene in recent times, have continued to attract attention to realize novel materials that are cheap and also have better properties. At a different level, encapsulating liquid crystals (LCs) in polymer networks not only adds mechanical strength, but could also result in device-based refractive index mismatch. Here, we describe a novel strategy combining the best of both these concepts to create graphene-incorporated polymer-stabilized LC (PSLC) devices.

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Bulk phase binary mixture of two rotator phase forming alkanes, n-tricosane (CH) and n-octacosane (CH), has been previously studied. CH exists in the R and R phases, whereas CH exists in the R and R phases. Over a certain range of composition, this binary mixture was found to exist in R, R and an intervening mesophase was reported to be the hexatic phase, wherein the long-range two-dimensional in-plane hexagonal lattice order of the R is lost and what remains is molecules present in hexagonal geometry without long-range positional correlation between individual hexagons.

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Morphology influences the functionality of covalent organic networks and determines potential applications. Here, we report for the first time the use of Zincke reaction to fabricate, under either solvothermal or microwave conditions, a viologen-linked covalent organic network in the form of hollow particles or nanosheets. The synthesized materials are stable in acidic, neutral, and basic aqueous solutions.

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A new type of optical storage device is described employing a material consisting of a host nematic liquid crystal, a photoisomerisable azobenzene component and a photopolymerizable monomer. The principle of image storing involves selectively controlling the birefringence of the medium immediately prior to photopolymerization of the monomer. We show that photoisomerisation driven nematic to isotropic transition can be employed to achieve this through proper timing of the reverse isomerization of the azobenzene compound before the nematic director fluctuations get quenched.

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Herein, we demonstrate that with the widespread theme of residue patterning and stereochemical restraints of self-complimenting proteinogenic amino acids, a new and rich class of homomeric dipeptides exhibiting two-dimensional fluid aggregates with hierarchical ordering can be obtained. In particular, a simple way of achieving a class of functional dipeptides, wherein the first and the second residues chosen are L-/D-alanines and L-/D-leucines, has been accomplished. The supramolecules synthesized can be regarded as intermediates between polycatenars and taper-shaped amphiphiles because they possess two lipophilic segments interlinked by a peptide unit (spacer).

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The phase transitional behavior of two homologous series of five-ring banana-shaped compounds comprising fluorine substituents synthesized through covalent linking of two chemically dissimilar rod-like anisometric cores (arms) to central 1,3-phenylene is reported. The novelty of these molecules originates from the fact that the molecules are highly nonsymmetrical. One of the arms, which is either salicylaldimine or Schiff base core, possesses two vicinal fluorine atoms at the terminal ring having a -decyloxy tail; while the -alkyl tail attached to the other arm was varied to realize a homologous series of compounds.

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The first mesoionic nematic and smectic A mesogens derived from sydnones that are characterized by both covalent and ionic features have been synthesized and evidenced by optical, calorimetric and X-ray diffraction studies.

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A new class of discotic liquid crystals derived from tris(N-salicylideneanilines) existing exclusively in their C3h and Cs keto-enamine tautomeric forms is reported. These compounds self-assemble to form columnar liquid crystalline phases with a small core-core separation as evidenced by X-ray diffraction studies.

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