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Yoshiki Chujo

Researcher Next ID · RN-035967

Researcher · Materials Science

Kyoto University

Kyoto, Japan

Accepting doctoral researchersFunding unknown
Works count
1,120
Citation count
30,445
H-index
81
i10-index
592

Research interests

Materials Science
Luminescence and Fluorescent Materials
Crystallization and Solubility Studies
X-ray Diffraction in Crystallography
Silicone and Siloxane Chemistry
Conducting polymers and applications

Publications

  • Recent Progress in the Development of Solid‐State Luminescent o‐Carboranes with Stimuli Responsivity

    Angewandte Chemie International Edition · 2020 · https://doi.org/10.1002/anie.201916666

  • Solid‐State Emission of the Anthracene‐ o ‐Carborane Dyad from the Twisted‐Intramolecular Charge Transfer in the Crystalline State

    Angewandte Chemie International Edition · 2016 · https://doi.org/10.1002/anie.201609656

  • o‐Carborane‐Based Anthracene: A Variety of Emission Behaviors

    Angewandte Chemie International Edition · 2015 · https://doi.org/10.1002/anie.201500129

  • Recent progress of optical functional nanomaterials based on organoboron complexes with β-diketonate, ketoiminate and diiminate

    NPG Asia Materials · 2015 · https://doi.org/10.1038/am.2015.118

  • New Polymeric Materials Based on Element-Blocks

    Bulletin of the Chemical Society of Japan · 2015 · https://doi.org/10.1246/bcsj.20150081

  • Mechanofluorochromic Materials Based on Aggregation‐Induced Emission‐Active Boron Ketoiminates: Regulation of the Direction of the Emission Color Changes

    Chemistry - A European Journal · 2015 · https://doi.org/10.1002/chem.201500033

  • Boron Diiminate with Aggregation‐Induced Emission and Crystallization‐Induced Emission‐Enhancement Characteristics

    Chemistry - A European Journal · 2014 · https://doi.org/10.1002/chem.201402946

  • Planar Chiral Tetrasubstituted [2.2]Paracyclophane: Optical Resolution and Functionalization

    Journal of the American Chemical Society · 2014 · https://doi.org/10.1021/ja412197j

  • Functionalization of Boron Diiminates with Unique Optical Properties: Multicolor Tuning of Crystallization-Induced Emission and Introduction into the Main Chain of Conjugated Polymers

    Journal of the American Chemical Society · 2014 · https://doi.org/10.1021/ja510985v

  • Highly Emissive Boron Ketoiminate Derivatives as a New Class of Aggregation‐Induced Emission Fluorophores

    Chemistry - A European Journal · 2013 · https://doi.org/10.1002/chem.201203703

  • Advanced Luminescent Materials Based on Organoboron Polymers

    Macromolecular Rapid Communications · 2012 · https://doi.org/10.1002/marc.201200239

  • Advanced functional materials based on polyhedral oligomeric silsesquioxane (POSS)

    Journal of Materials Chemistry · 2011 · https://doi.org/10.1039/c1jm14231c

  • Multicolor Tuning of Aggregation-Induced Emission through Substituent Variation of Diphenyl-o-carborane

    The Journal of Organic Chemistry · 2010 · https://doi.org/10.1021/jo101999b

  • Emission via Aggregation of Alternating Polymers with o-Carborane and p-Phenylene−Ethynylene Sequences

    Macromolecules · 2009 · https://doi.org/10.1021/ma8027358

  • π-Conjugated Organoboron Polymers via the Vacant p-Orbital of the Boron Atom

    Polymer Journal · 2007 · https://doi.org/10.1295/polymj.pj2007170

  • Organic polymer hybrids with silica gel formed by means of the sol-gel method

    Advances in polymer science · 2006 · https://doi.org/10.1007/bfb0051634

  • Through‐Space Conjugated Polymers Based on Cyclophanes

    Angewandte Chemie International Edition · 2006 · https://doi.org/10.1002/anie.200600752

  • Synthesis of Gold Nanoparticles Modified with Ionic Liquid Based on the Imidazolium Cation

    Journal of the American Chemical Society · 2004 · https://doi.org/10.1021/ja039895g

  • Effect of Anionic Starburst Dendrimers on the Crystallization of CaCO3 in Aqueous Solution: Size Control of Spherical Vaterite Particles

    Langmuir · 2002 · https://doi.org/10.1021/la011345d

  • Control of Crystal Nucleation and Growth of Calcium Carbonate by Synthetic Substrates

    Chemistry of Materials · 2001 · https://doi.org/10.1021/cm011035g

  • Thermally Reversible IPN Organic−Inorganic Polymer Hybrids Utilizing the Diels−Alder Reaction

    Macromolecules · 2000 · https://doi.org/10.1021/ma991899b

  • Extension of π-Conjugation Length via the Vacant p-Orbital of the Boron Atom. Synthesis of Novel Electron Deficient π-Conjugated Systems by Hydroboration Polymerization and Their Blue Light Emission

    Journal of the American Chemical Society · 1998 · https://doi.org/10.1021/ja9741943

  • Organic—inorganic hybrid materials

    Current Opinion in Solid State and Materials Science · 1996 · https://doi.org/10.1016/s1359-0286(96)80105-7

  • Reversible gelation of polyoxazoline by means of Diels-Alder reaction

    Macromolecules · 1990 · https://doi.org/10.1021/ma00212a007

  • Facile generation of a reactive palladium(II) enolate intermediate by the decarboxylation of palladium(II) .beta.-ketocarboxylate and its utilization in allylic acylation

    Journal of the American Chemical Society · 1980 · https://doi.org/10.1021/ja00540a053

Current projects

    No projects listed.