About: Yoshiaki Shoji

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0001-8437-1965)

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) 研究者 (zh) հետազոտող (hy) researcher (ORCID 0000-0001-8437-1965) (en)
rdfs:label	Yoshiaki Shoji (en) Yoshiaki Shoji (es) Yoshiaki Shoji (nl) Yoshiaki Shoji (sl) Yoshiaki Shoji (ast) 庄子良晃 (ja)
skos:prefLabel	Yoshiaki Shoji (en) Yoshiaki Shoji (es) Yoshiaki Shoji (nl) Yoshiaki Shoji (sl) Yoshiaki Shoji (ast) 庄子良晃 (ja)
name	Yoshiaki Shoji (en) Yoshiaki Shoji (es) Yoshiaki Shoji (nl) Yoshiaki Shoji (sl) Yoshiaki Shoji (ast) 庄子良晃 (ja)
given name	wds:Q51189525-8cd217f1-49f7-8613-6e7a-8e0bd97257f7
given name	Yoshiaki
instance of	wds:Q51189525-647DBEE8-B43A-4AFA-8F96-760F7EF989CC
instance of	Homo sapiens
Researchmap ID	wds:Q51189525-6CEDFF7B-A726-4CFE-B8AE-920C62AC6ADA
Researchmap ID	7000017720
occupation	wds:Q51189525-570D0B72-5040-4C6C-9D49-697737C73A82
employer	wds:Q51189525-337EB657-419F-435F-BB08-DF1462B16EAF wds:Q51189525-836814D5-4CD1-4FF2-9F8E-D58212EA9D16
CiNii Research ID	wds:Q51189525-921B8DF9-0F85-4E97-9546-EC227B1FABDD
family name	wds:Q51189525-febae586-4d9d-6e43-f027-a3606d122c82
J-GLOBAL ID	wds:Q51189525-BA02CB0A-5640-4F15-AD5A-253632CE1333
CiNii Research ID	https://cir.nii.ac.jp/crid/1420282801208562688.rdf
occupation	researcher
employer	RIKEN Tokyo Institute of Technology
CiNii Research ID	1420282801208562688
family name	Shoji
J-GLOBAL ID	201601013226910520
ORCID iD	wds:Q51189525-E4DB8A43-E922-4F97-91DC-AFD708794A5C
ORCID iD	https://orcid.org/0000-0001-8437-1965
ORCID iD	0000-0001-8437-1965
e-Rad researcher number	wds:Q51189525-210F0073-15CE-4C95-B0CE-A769BFD448D3
e-Rad researcher number	40525573
ResearcherID	wds:Q51189525-D97117AC-51BA-421A-85C2-D562283BFBC8
Publons author ID	wds:Q51189525-ac9944a5-9ab1-4bcf-a952-83ab6f60bd0d
ResearcherID	D-4672-2014
Publons author ID	1367204
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q51189525
is author of	Sensing of chiral fullerenes by a cyclic host with an asymmetrically distorted pi-electronic component. Boron-mediated sequential alkyne insertion and C-C coupling reactions affording extended π-conjugated molecules. A stable doubly hydrogen-bridged butterfly-shaped diborane(4) compound Selective extraction of higher fullerenes using cyclic dimers of zinc porphyrins. The molecular and electronic structures of a thioaroyl cation formed by borinium ion-mediated C=S double bond cleavage of CS2. A two-coordinate boron cation featuring C-B+-C bonding. Unveiling a New Aspect of Simple Arylboronic Esters: Long-Lived Room-Temperature Phosphorescence from Heavy-Atom-Free Molecules. An Isolable Diborane(4) Compound with Terminal B–H Bonds: Structural Characteristics and Electronic Properties Synthesis and Structures of a Series of Bulky “Rind-Br” Based on a Rigid Fused-Rings-Hydrindacene Skeleton Mechanistic Study of Highly Efficient Direct 1,2-Carboboration of Alkynes with 9-Borafluorenes Induced-fit expansion and contraction of a self-assembled nanocube finely responding to neutral and anionic guests Synthesis and Reactivity of Cyclic Borane-Amidine Conjugated Molecules Formed by Direct 1,2-Carboboration of Carbodiimides with 9-Borafluorenes Chirality sensing of fullerenes using cyclic hosts having a chiral N-substituted porphyrin: a remote substituent effect. Formation of an Isolable Divinylborinium Ion through Twofold 1,2-Carboboration between a Diarylborinium Ion and Diphenylacetylene. Boron–Boron σ-Bond Formation by Two-Electron Reduction of a H-Bridged Dimer of Monoborane Supramolecular Scaffold for Tailoring the Two-Dimensional Assembly of Functional Molecular Units into Organic Thin Films. Rational synthesis of organic thin films with exceptional long-range structural integrity (11)B Solid-State NMR Interaction Tensors of Linear Two-Coordinate Boron: The Dimesitylborinium Cation Back Cover: Formation of an Isolable Divinylborinium Ion through Twofold 1,2-Carboboration between a Diarylborinium Ion and Diphenylacetylene (Angew. Chem. Int. Ed. 19/2017) One-pot enantioselective extraction of chiral fullerene C76 using a cyclic host carrying an asymmetrically distorted, highly pi-basic porphyrin module A few-layer molecular film on polymer substrates to enhance the performance of organic devices. Chiral crystal-like droplets displaying unidirectional rotational sliding Ultralow-Noise Organic Transistors Based on Polymeric Gate Dielectrics with Self-Assembled Modifiers Electric-Field-Controllable Conductance Switching of an Overcrowded Ethylene Self-Assembled Monolayer Synthesis and Catalytic Applications of a Triptycene-Based Monophosphine Ligand for Palladium-Mediated Organic Transformations Convenient Route to Monocarba-closo-dodecaborate Anions Supramolecular scaffolds enabling the controlled assembly of functional molecular units. Hexathioalkyl sumanenes: an electron-donating buckybowl as a building block for supramolecular materials. Triptycene Tripods for the Formation of Highly Uniform and Densely Packed Self-Assembled Monolayers with Controlled Molecular Orientation Sensing the chirality of various organic solvents by helically arranged π-blades Highly-ordered Triptycene Modifier Layer Based on Blade Coating for Ultraflexible Organic Transistors An Organic Borate Salt with Superior p-Doping Capability for Organic Semiconductors A Theoretical Study on the Mechanism of the Oxidative Deborylation/C-C Coupling Reaction of Borepin Derivatives Room-Temperature Pentacene Fluids: Oligoethylene Glycol Substituent-Controlled Morphologies and Singlet Fission
is author of	wds:Q46693789-B76F9AB8-72FE-44E4-8700-532B4F9DC0D8 wds:Q59441559-952BFEB8-7501-4560-AE58-D0F747B4B5DB wds:Q59441605-C674D6DA-F9C2-4DDD-A409-B57F69FC6F20 wds:Q51671263-DE23040A-E211-44BB-BE30-EA25CA0CE50D wds:Q57702624-DF30FB48-BA04-41EB-B2EC-4F1C6E3AF912 wds:Q91331202-384419EF-A144-4DA8-BD15-A039B55EE1E9 wds:Q51189458-97552DB6-B439-43B8-878D-3815EA2B1208 wds:Q57702660-D1DA9647-ABA5-4218-8E69-6ECCB77D9E2F

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