about
Boron Difluoride Complexes of Expanded N-Confused Calix[n]phyrins That Demonstrate Unique Luminescent and Lasing Properties.Tetrathiafulvalene- (TTF-) Derived Oligopyrrolic Macrocycles.Synthesis of a Neo-Confused Octaphyrin and the Formation of Its Mononuclear Complexes.Protonation-induced formation of a stable singlet biradicaloid derived from a modified sapphyrin analogue.A porphyrin-related macrocycle with an embedded 1,10-phenanthroline moiety: fluorescent magnesium(II) ion sensor.A p-quinodimethane-bridged porphyrin dimer.Tetracyanoquaterrylene and tetracyanohexarylenequinodimethanes with tunable ground states and strong near-infrared absorption.Pushing extended p-quinodimethanes to the limit: stable tetracyano-oligo(N-annulated perylene)quinodimethanes with tunable ground states.Bis-Copper(II)/π-Radical Multi-Heterospin System with Non-innocent Doubly N-Confused Dioxohexaphyrin(1.1.1.1.1.0) Ligand.Singly and Doubly N-Confused Calix[4]phyrin Organoplatinum(II) Complexes as Near-IR Triplet Sensitizers.Structural, Photophysical, and Magnetic Circular Dichroism Studies of Three Rigidified meso-Pentafluorophenyl-Substituted Hexaphyrin Analogues.A Diradical Approach towards BODIPY-Based Dyes with Intense Near-Infrared Absorption around λ=1100 nm.Formation of Ground State Triplet Diradicals from Annulated Rosarin Derivatives by Triprotonation.Stable π Radical from a Contracted Doubly N-Confused Hexaphyrin by Double Palladium Metalation.Intramolecular charge transfer character in tetrathiafulvalene-annulated porphyrinoids: effects of core modification and protonation.Spectroscopic and theoretical studies of acid-base behaviors of N-confused porphyrins: effects of meso-aryl substituents.Cyclo[6]pyridine[6]pyrrole: a dynamic, twisted macrocycle with no meso bridges.Stereoretentive Ligand Exchange Reactions of N-Fused Porphyrin Ruthenium(II) Complexes.Doubly N-Confused [36]Octaphyrin(1.1.1.1.1.1.1.1): Isomerization, Bis-Metal Coordination, and Topological Chirality.Tautomerism-Induced Cis-Trans Isomerization of Pyridylethenyl N-Confused Porphyrin.Organometallic Group 11 (CuIII , AgIII , AuIII ) Complexes of a trans-Doubly N-Confused Porphyrin: An "Expanded Imidazole" Structural Motif.Switch-ON Near IR Fluorescent Dye Upon Protonation: Helically Twisted Bis(Boron Difluoride) Complex of π-Extended Corrorin.Macrocyclic Transformations from Norrole to Isonorrole and an N-Confused Corrole with a Fused Hexacyclic Ring System Triggered by a Pyrrole Substituent.Photophysical analysis of 1,10-phenanthroline-embedded porphyrin analogues and their magnesium(II) complexes.Breaking aggregation in a tetrathiafulvalene-fused zinc porphyrin by metal-ligand coordination to form a donor-acceptor hybrid for ultrafast charge separation and charge stabilization.Near-Infrared Phosphorescent Iridium(III) Benzonorrole Complexes Possessing Pyridine-based Axial Ligands.Fully Fused Quinoidal/Aromatic Carbazole Macrocycles with Poly-radical Characters.2-(Naphthalen-1-yl)thiophene as a New Motif for Porphyrinoids: Meso-Fused Carbaporphyrin.Two Discrete RuCp* (Cp*=Pentamethylcyclopentadienyl) Binding Modes of N-Confused Porphyrins: Peripheral π Complex and Sitting Atop Ruthenocenophane Complex by Skeletal Transformation.Protonation-coupled redox reactions in planar antiaromatic meso-pentafluorophenyl-substituted o-phenylene-bridged annulated rosarins.Stable tetrabenzo-Chichibabin's hydrocarbons: tunable ground state and unusual transition between their closed-shell and open-shell resonance forms.Ground-State Copper(III) Stabilized by N-Confused/N-Linked Corroles: Synthesis, Characterization, and Redox ReactivityBis-copper(II) Complex of Triply-linked Corrole Dimer and Its DicationPorphyrin/Platinum(II) C^N^N Acetylide Complexes: Synthesis, Photophysical Properties, and Singlet Oxygen GenerationNear-infrared-induced electron transfer of an uranyl macrocyclic complex without energy transfer to dioxygenPorphyrins Fused with Strongly Electron-Donating 1,3-Dithiol-2-ylidene Moieties: Redox Control by Metal Cation Complexation and Anion BindingTetrathiafulvalene-annulated [28]hexaphyrin(1.1.1.1.1.1): a multi-electron donor system subject to conformational controlCyclo[m]pyridine[n]pyrroles: hybrid macrocycles that display expanded π-conjugation upon protonationNeutral radical and singlet biradical forms of meso-free, -keto, and -diketo hexaphyrins(1.1.1.1.1.1): effects on aromaticity and photophysical propertiesComparative electrochemical and photophysical studies of tetrathiafulvalene-annulated porphyrins and their Zn(II) complexes: the effect of metalation and structural variation
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Q36105248-A72A65A3-1866-4D3A-BC74-34AB80B86C53Q38983756-15D1EDC5-90B0-4564-90C0-0C99C7963F45Q40541279-72501228-8F77-48C9-9329-F33655E373E7Q42969743-246DB433-D6BC-4D0F-ABB5-75DB8DD8F879Q43233263-245C5DB6-DF08-4CB2-89F7-79FC108E741BQ43749927-3BF7882C-07DB-48D1-B03F-5C06A3DFC664Q44033532-C5A6B93D-9907-442B-B6E4-407B693C3F38Q45773319-9DA31937-B6EB-4F69-BA71-336BEBCC81D7Q46307090-117F7689-6A2C-470E-8C5D-F41B5AA70A54Q46330483-35CE212F-44BF-464F-BE1C-B27FFE8EA087Q46401874-1DA9BF11-BD17-4DCF-A6A4-AD1D0493276DQ46605843-7C1EBF10-5B8B-46FC-B492-5D3A75BB2533Q46696207-EF66578F-9CF5-4727-A042-AEAC2648EBE0Q46731749-DD2AF4A0-4644-4C11-834C-457360F19B35Q46764570-A66C032D-735E-43E7-89F6-3A8B8DA5F092Q46786608-931AE500-140A-4A91-BE31-A3C0B66A4D9DQ46895871-35BDEF28-0522-4405-8D9B-36E15A3EEDD6Q47628114-C7174C3C-B022-4AE6-975E-6F27ECAEAAC5Q47663892-D3453B25-FBD5-411D-915C-B63B60FA8D41Q47879427-993FAEA6-64A5-4EE5-87E9-7DA8F115484CQ48020265-538DB2A3-EAFC-4E4E-B640-F9B99A7E58D4Q49848907-B185523E-80AC-40AE-8B04-632B57920D70Q50043528-BCD155EE-1034-4477-8837-48CDC2D022E4Q50502978-6DFFE2F3-2E8D-4E77-968B-E2984D038852Q51036472-D78090AE-A0B4-4293-B033-7BE87FB5D535Q51308835-C5B8FE56-02DC-4655-AEB4-04A8BE2F01A5Q51309279-0B358192-3DC4-4A86-9986-84C441A0D586Q51501146-B2B8D840-D609-4172-BAFA-DD852F0A1795Q52357748-80FEEE30-E1D2-4E81-9117-25C4F64D1E31Q53349506-BA200B81-15A8-421B-AEA3-327AF0E2F28BQ54100871-8FC7DA24-C0B7-4CF2-8517-DE8971937A9FQ58227286-06E52870-9175-4026-88A2-5CA95E3FAEA9Q58590230-37B6006A-64F2-4EF4-AA93-BE02B23AA9B1Q59264400-ED5038E3-2CFA-40B3-A9E3-DB938ADF23DEQ62272642-478A4E1C-0116-4359-B6DD-6E62ACB7B24DQ62272683-BCB8CC35-F52B-4006-AF06-4F6F6F62DFA4Q62272687-BEEA82C5-E40C-482B-B03E-4476631B042BQ83443671-60686162-32A1-4022-890F-920EDD473E5CQ84856786-AFF5A589-19C6-4ED1-B017-D12ECA7CCD2FQ85528019-FA8D48ED-8DB5-4019-9E86-1C1625E20030
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Masatoshi Ishida
@ast
Masatoshi Ishida
@en
Masatoshi Ishida
@es
Masatoshi Ishida
@nl
Masatoshi Ishida
@sl
type
label
Masatoshi Ishida
@ast
Masatoshi Ishida
@en
Masatoshi Ishida
@es
Masatoshi Ishida
@nl
Masatoshi Ishida
@sl
prefLabel
Masatoshi Ishida
@ast
Masatoshi Ishida
@en
Masatoshi Ishida
@es
Masatoshi Ishida
@nl
Masatoshi Ishida
@sl
P1053
F-1199-2016
P106
P1153
35326911400
P21
P31
P3829
P496
0000-0002-1117-2188