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Inna K. Shundrina

Researcher at Russian Academy of Sciences

Publications -  76
Citations -  658

Inna K. Shundrina is an academic researcher from Russian Academy of Sciences. The author has contributed to research in topics: Phenylene & Chemistry. The author has an hindex of 12, co-authored 68 publications receiving 456 citations. Previous affiliations of Inna K. Shundrina include Novosibirsk State University.

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Synthesis and thermomechanical properties of hybrid photopolymer films based on the thiol-siloxane and acrylate oligomers

TL;DR: In this paper, the synthesis of hybrid oligomers for photopolymer compositions was carried out based on the thiol-ene reaction between the tetraacrylate dihydroxydiphenylsulfide derivative and Thiol-siloxane oligomer.
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Synthesis and characterization of novel fluorinated pyridine-based polyimides

TL;DR: In this article, pyridine-containing polyimides based on fluorinated γ-Х-pyridylenediamines and dianhydride 6FDA were prepared by one-step polycondensation in benzoic acid melt.
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Crystal packing control of a trifluoromethyl‐substituted furan/phenylene co‐oligomer

TL;DR: Terminal trifluoromethyl groups induce weak intermolecular interactions which control the crystal packing and optical properties of co-oligomer single crystals, which exhibit high photoluminescence efficiency and have optical properties which strongly depend on the crystalpacking.
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Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology

TL;DR: In this article, the effect of the synthesis conditions on the size and morphology of the nanoparticles obtained via the reduction of silver ions by benzyl alcohol in the presence of carboxylated methoxypolyethylene glycols with different molecular weights was studied.
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Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states.

TL;DR: A new synthetic methodology based on the self-condensation of 1,2,3-benzodithiazolyl diradicals (Herz radicals) produces unprecedented 5-6-6 -6-5 and 5- 6-7-6,5 pentacyclic sulfur-nitrogen near-IR dyes featuring up to five multiple long-lived and differently coloured redox-states.