研究紹介
研究テーマ
Investigation of Structural, Physical and Functional Properties of Aliphatic Polyketones a.k.a. Carbonyl Ropes
キーワード
organic synthesis, non-covalent interactions, functional organic materials, porous frameworks, stable organic radicals, paramagnetic liquid crystals
経歴
経歴書を参照願います。
代表的な研究成果
- A Hydrogen-Bonded Organic Framework Based on Redox-Active Tri(dithiolylidene)cyclohexanetrione
K. I. Shivakumar, S-i. Noro, Y. Yamaguchi, Y. Ishigaki, A. Saeki, K. Takahashi, T. Nakamura, I. Hisaki, Chem. Commun. 2021, 57, 1157-1160
DOI: 10.1039/D0CC07776C - Photoconductive Bent-Core Liquid Crystalline Radicals with a Paramagnetic Polar Switchable Phase
K. I. Shivakumar, D. Pociecha, J. Szczytko, S. Kapuscinski, H. Monobe, P. Kaszynski, J. Mater. Chem. C, 2020, 8, 1083-1088
DOI: 10.1039/C9TC05764A - Conducting Nanofibres of Solvatofluorochromic Cyclohexanetrione–Dithiolylidene-Based C3 Symmetric Molecule
K. I. Shivakumar, Goudappagouda; R. Gonnade, S. S. Babu, G. J. Sanjayan, Chem. Commun. 2018, 54, 212-215
DOI: 10.1039/C7CC08741A - Mixed-Stack Charge Transfer Crystals of Pillar[5]quinone and Tetrathiafulvalene Exhibiting Ferroelectric Features
K. I. Shivakumar, K. Swathi, Goudappagouda, T. Das, A. Kumar, R.D. Makde, K. Vanka, K. S. Narayan, S. S. Babu, G. J. Sanjayan, Chem. Eur. J. 2017, 23, 12630-12635.
DOI: 10.1002/chem.201702577 - Exploiting Powder X-ray Diffraction to Establish the Solvent-Assisted Solid-State Supramolecular Assembly of Pillar[5]quinone
K. I. Shivakumar, Y. Yan, C. E. Hughes, D. C. Apperley, K. D. M. Harris, G. J. Sanjayan, Cryst. Growth Des., 2015, 15, 1583-1587.
DOI: 10.1021/acs.cgd.5b00277
関連する研究記事
業績一覧
2022年
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Determination of the Critical Chain Length for Macromolecular Crystallization Using Structurally Flexible Polyketones
, Y. Manabe, Y. Inaba, Y. Kinoshita, J. Pirillo, Y. Hijikata, T. Yoneda, K. I. Shivakumar, S. Tanaka, H. Asakawa, Y. Inokuma, Chem. Sci., 2022, 13, 9848-9854
DOI: 10.1039/d2sc03083g
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Alkali Metal Ion Binding Using Cyclic Polyketones
, K. I. Shivakumar, M. Murugavel, Y. Inaba, T. Yoneda, Y. Ide, J. Pirillo, Y. Hijikata, Y. Inokuma, Chem. Commun., 2022, 58, 2971-2974
DOI: 10.1039/d2cc00361a