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Aromaticity Switching in Porphyrinoids
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3757(19980116)110:1/2<187::aid-ange187>3.0.co;2-8openalex-snapshot
Globale und lokale Aromatizität in Porphyrinen: eine Analyse anhand von Molekülgeometrien und kernunabhängigen chemischen Verschiebungen
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19980202)37:1/2<177::aid-anie177>3.0.co;2-hopenalex-snapshot
Global and Local Aromaticity in Porphyrins: An Analysis Based on Molecular Geometries and Nucleus-Independent Chemical Shifts
inferredcites →https://doi.org/10.1002/(sici)1522-2675(19990113)82:1<59::aid-hlca59>3.0.co;2-8openalex-snapshot
Konfigurations- und konformationsisomere paratrope, rotationsdynamische Tetraepoxy[32]annulene(6.2.6.2) und diatrope Tetraoxa[30]porphyrin(6.2.6.2)-Dikationen: Nachweis eines Tetraepoxy[31]annulen(6.2.6.2)-Radikalkations
inferredcites →https://doi.org/10.1002/(sici)1522-2675(20000216)83:2<495::aid-hlca495>3.0.co;2-3openalex-snapshot
Superheteroaromaten mit Furan-Bausteinen: Isomere antiaromatische Tetraepoxy[36]annulene(6.4.6.4) und aromatische Tetraoxa[34]porphyrin(6.4.6.4)-Dikationen
inferredcites →https://doi.org/10.1002/1521-3765(20011203)7:23<5099::aid-chem5099>3.0.co;2-mopenalex-snapshot
Figure-Eight Tetrathiaoctaphyrin and Dihydrotetrathiaoctaphyrin
inferredcites →https://doi.org/10.1002/1521-3765(20011203)7:23<5113::aid-chem5113>3.0.co;2-vopenalex-snapshot
Tetraphenylbenziporphyrin—A Ligand for Organometallic Chemistry
inferredcites →https://doi.org/10.1002/1521-3765(20021202)8:23<5403::aid-chem5403>3.0.co;2-copenalex-snapshot
A Direct Link between Annulene and Porphyrin Chemistry—21-Vacataporphyrin
inferredcites →https://doi.org/10.1002/1522-2675(20010711)84:7<2022::aid-hlca2022>3.0.co;2-hopenalex-snapshot
Tetraepoxy[32]annulene(4.4.4.4) und `Tetraoxa[30]porphyrin(4.4.4.4)'-Dikationen
inferredcites →https://doi.org/10.1002/1522-2675(20010711)84:7<2037::aid-hlca2037>3.0.co;2-mopenalex-snapshot
Neutrale aromatische Tetraepoxyannulene: Tetraepoxy[26]annulene(4.2.2.2) und Tetraepoxy[30]annulene(4.4.4.2) - Systeme mit hoher molekularer Dynamik
inferredcites →https://doi.org/10.1002/ange.19881000340openalex-snapshot
Tetraoxaporphyrinogen (Tetraoxaquateren): Oxidation zum Tetraoxaporphyrin‐Dikation
inferredcites →https://doi.org/10.1002/ange.19941060226openalex-snapshot
Neue Pyridin enthaltende porphyrinoide Makrocyclen
inferredcites →https://doi.org/10.1002/ange.19941061107openalex-snapshot
Tetraoxa[22]porphyrin(2.2.2.2)‐Dikation und Tetraoxa[24]porphyrinogen(2.2.2.2)
inferredcites →https://doi.org/10.1002/ange.19941061230openalex-snapshot
Benziporphyrin, ein Benzol enthaltendes, nicht aromatisches Porphyrinanalogon
inferredcites →https://doi.org/10.1002/ange.19951072210openalex-snapshot
Oxybenziporphyrin, ein vollständig aromatisches Semichinon‐Porphyrin‐Analogon mit Delokalisierungsmöglichkeiten für 18 π‐Elektronen
inferredcites →https://doi.org/10.1002/ange.200200561openalex-snapshot
Synthesechemie expandierter Porphyrine
inferredcites →https://doi.org/10.1002/ange.200353189openalex-snapshot
Oxidative Metalation of Azuliporphyrins with Copper( II ) Salts: Formation of a Porphyrin Analogue System with a Unique Fully Conjugated Nonaromatic Azulene Subunit
inferredcites →https://doi.org/10.1002/ange.200501635openalex-snapshot
Dithiaethyneporphyrin: An Atypical [18]Triphyrin(4.1.1) Frame for Contracted Porphyrins
inferredcites →https://doi.org/10.1002/ange.200503426openalex-snapshot
Tribenzosubporphines: Synthesis and Characterization
inferredcites →https://doi.org/10.1002/ange.200600589openalex-snapshot
Subpyriporphyrin—A [14]Triphyrin(1.1.1) Homologue with an Embedded Pyridine Moiety
inferredcites →https://doi.org/10.1002/ange.200700555openalex-snapshot
Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch
inferredcites →https://doi.org/10.1002/ange.200704407openalex-snapshot
Metalation of Expanded Porphyrins: A Chemical Trigger Used To Produce Molecular Twisting and Möbius Aromaticity
inferredcites →https://doi.org/10.1002/ange.200804457openalex-snapshot
Protonation‐Triggered Conformational Changes to Möbius Aromatic [32]Heptaphyrins(1.1.1.1.1.1.1)
inferredcites →https://doi.org/10.1002/ange.201001765openalex-snapshot
Möbius Antiaromatic Bisphosphorus Complexes of [30]Hexaphyrins
inferredcites →https://doi.org/10.1002/ange.201003353openalex-snapshot
Figure‐Eight‐Strukturen, Möbius‐Bänder und mehr: Konformation und Aromatizität von Porphyrinoiden
inferredcites →https://doi.org/10.1002/ange.201004015openalex-snapshot
π Conjugation Transmitted across a d‐Electron Metallocene in Ferrocenothiaporphyrin Macrocycles
inferredcites →https://doi.org/10.1002/ange.201109038openalex-snapshot
From 21,23‐Dioxaporphyrin to a 3‐Pyranone Dioxacorrole Skeleton: The Achmatowicz Rearrangement in the Porphyrin Frame
inferredcites →https://doi.org/10.1002/ange.201204395openalex-snapshot
Gram‐Scale Synthesis of Nickel(II) Norcorrole: The Smallest Antiaromatic Porphyrinoid
inferredcites →https://doi.org/10.1002/ange.201208289openalex-snapshot
Ruthenocenoporphyrinoids: Conformation Determines Macrocyclic π Conjugation Transmitted Across a d‐Electron Metallocene
inferredcites →https://doi.org/10.1002/ange.201209678openalex-snapshot
Thiatriphyrin(2.1.1): A Core‐Modified Contracted Porphyrin
inferredcites →https://doi.org/10.1002/ange.201310129openalex-snapshot
Synthesis and Switching the Aromatic Character of Oxatriphyrins(2.1.1)
inferredcites →https://doi.org/10.1002/ange.201310374openalex-snapshot
An Antiaromatic Electrode‐Active Material Enabling High Capacity and Stable Performance of Rechargeable Batteries
inferredcites →https://doi.org/10.1002/ange.201403372openalex-snapshot
Reversible Redox Reaction Between Antiaromatic and Aromatic States of 32π‐Expanded Isophlorins
inferredcites →https://doi.org/10.1002/ange.201406893openalex-snapshot
An Amphoteric Switch to Aromatic and Antiaromatic States of a Neutral Air‐Stable 25π Radical
inferredcites →https://doi.org/10.1002/anie.198804091openalex-snapshot
Tetraoxaporphyrinogen (Tetraoxaquaterene): Oxidation to the Tetraoxaporphyrin Dication
inferredcites →https://doi.org/10.1002/anie.199402191openalex-snapshot
New Porphyrinoid Macrocycles Containing Pyridine
inferredcites →https://doi.org/10.1002/anie.199411511openalex-snapshot
Tetraoxa[22]porphyrin(2.2.2.2) Dication and Tetraoxa[24]porphyrinogens(2.2.2.2)
inferredcites →https://doi.org/10.1002/anie.199412461openalex-snapshot
Benziporphyrin, a Benzene‐Containing, Nonaromatic Porphyrin Analogue
inferredcites →https://doi.org/10.1002/anie.199525331openalex-snapshot
Oxybenziporphyrin, a Fully Aromatic Semiquinone Porphyrin Analog with Pathways for 18π‐Electron Delocalization
inferredcites →https://doi.org/10.1002/anie.200200561openalex-snapshot
Synthetic Expanded Porphyrin Chemistry
inferredcites →https://doi.org/10.1002/anie.200353189openalex-snapshot
Oxidative Metalation of Azuliporphyrins with Copper( II ) Salts: Formation of a Porphyrin Analogue System with a Unique Fully Conjugated Nonaromatic Azulene Subunit
inferredcites →https://doi.org/10.1002/anie.200501635openalex-snapshot
Dithiaethyneporphyrin: An Atypical [18]Triphyrin(4.1.1) Frame for Contracted Porphyrins
inferredcites →https://doi.org/10.1002/anie.200503426openalex-snapshot
Tribenzosubporphines: Synthesis and Characterization
inferredcites →https://doi.org/10.1002/anie.200600589openalex-snapshot
Subpyriporphyrin—A [14]Triphyrin(1.1.1) Homologue with an Embedded Pyridine Moiety
inferredcites →https://doi.org/10.1002/anie.200700555openalex-snapshot
Expanded Porphyrin with a Split Personality: A Hückel–Möbius Aromaticity Switch
inferredcites →https://doi.org/10.1002/anie.200704407openalex-snapshot
Metalation of Expanded Porphyrins: A Chemical Trigger Used To Produce Molecular Twisting and Möbius Aromaticity
inferredcites →https://doi.org/10.1002/anie.200804457openalex-snapshot
Protonation‐Triggered Conformational Changes to Möbius Aromatic [32]Heptaphyrins(1.1.1.1.1.1.1)
inferredcites →https://doi.org/10.1002/anie.201001765openalex-snapshot
Möbius Antiaromatic Bisphosphorus Complexes of [30]Hexaphyrins
inferredcites →https://doi.org/10.1002/anie.201003353openalex-snapshot
Figure Eights, Möbius Bands, and More: Conformation and Aromaticity of Porphyrinoids
inferredcites →https://doi.org/10.1002/anie.201004015openalex-snapshot
π Conjugation Transmitted across a d‐Electron Metallocene in Ferrocenothiaporphyrin Macrocycles
inferredcites →https://doi.org/10.1002/anie.201109038openalex-snapshot
From 21,23‐Dioxaporphyrin to a 3‐Pyranone Dioxacorrole Skeleton: The Achmatowicz Rearrangement in the Porphyrin Frame
inferredcites →https://doi.org/10.1002/anie.201204395openalex-snapshot
Gram‐Scale Synthesis of Nickel(II) Norcorrole: The Smallest Antiaromatic Porphyrinoid
inferredcites →https://doi.org/10.1002/anie.201208289openalex-snapshot
Ruthenocenoporphyrinoids: Conformation Determines Macrocyclic π Conjugation Transmitted Across a d‐Electron Metallocene
inferredcites →https://doi.org/10.1002/anie.201209678openalex-snapshot
Thiatriphyrin(2.1.1): A Core‐Modified Contracted Porphyrin
inferredcites →https://doi.org/10.1002/anie.201310129openalex-snapshot
Synthesis and Switching the Aromatic Character of Oxatriphyrins(2.1.1)
inferredcites →https://doi.org/10.1002/anie.201310374openalex-snapshot
An Antiaromatic Electrode‐Active Material Enabling High Capacity and Stable Performance of Rechargeable Batteries
inferredcites →https://doi.org/10.1002/anie.201403372openalex-snapshot
Reversible Redox Reaction Between Antiaromatic and Aromatic States of 32π‐Expanded Isophlorins
inferredcites →https://doi.org/10.1002/anie.201406893openalex-snapshot
An Amphoteric Switch to Aromatic and Antiaromatic States of a Neutral Air‐Stable 25π Radical
inferredcites →https://doi.org/10.1002/anie.201410595openalex-snapshot
Oxatriphyrins(2.1.1) Incorporating an ortho‐Phenylene Motif
inferredcites →https://doi.org/10.1002/chem.19950010111openalex-snapshot
5,10,15,20‐Tetraphenylsapphyrin‐Identification of a Pentapyrrolic Expanded Porphyrin in the Rothemund Synthesis
inferredcites →https://doi.org/10.1002/chem.19970030216openalex-snapshot
Nickel Complexes of 21‐Oxaporphyrin and 21, 23‐Dioxaporphyrin
inferredcites →https://doi.org/10.1002/chem.200400787openalex-snapshot
Synthesis, Characterization, and Properties of Subporphyrazines: A New Class of Nonplanar, Aromatic Macrocycles with Absorption in the Green Region
inferredcites →https://doi.org/10.1002/chem.200900841openalex-snapshot
N‐Fusion Approach in Construction of Contracted Carbaporphyrinoids: Formation of N‐Fused Telluraporphyrin
inferredcites →https://doi.org/10.1002/chem.200902708openalex-snapshot
Phosphorus Complexes of the First Expanded Isophlorins
inferredcites →https://doi.org/10.1002/chem.201101061openalex-snapshot
The Chemistry of Unstable Molecules with Unusual Electronic Structures : Anti-aromatic 16π Porphyrins and Cyclic Aromatic Remote Carbenes
inferredcites →https://doi.org/10.1002/chem.201303676openalex-snapshot
Hückel and Möbius Expanded para‐Benziporphyrins: Synthesis and Aromaticity Switching
inferredcites →https://doi.org/10.1002/chem.201404570openalex-snapshot
Reversible Reduction of Oxatriphyrin(3.1.1)—Adjusting the Coordination Abilities to the Central Ion
inferredcites →https://doi.org/10.1002/ejoc.200600364openalex-snapshot
Pyriporphyrin – A Porphyrin Homologue Containing A Built‐in Pyridine Moiety
inferredcites →https://doi.org/10.1002/ejoc.201300377openalex-snapshot
Expanded Triphyrin Derived from a Carbacorrole Architecture
inferredcites →https://doi.org/10.1002/hlca.19970800103openalex-snapshot
Konfigurations‐ und konformationsisomere antiaromatische [28]Tetraoxaporphyrinoide(4.2.4.2) und aromatische [26]Tetraoxaporphyrin(4.2.4.2)‐dikationen. Eine neue Form molekularer Dynamik in makrocyclischen Systemen
inferredcites →https://doi.org/10.1007/978-3-540-68343-8_3openalex-snapshot
Aromaticity and Tautomerism in Porphyrins and Porphyrinoids
inferredcites →https://doi.org/10.1021/cr0101454openalex-snapshot
Subphthalocyanines: Singular Nonplanar Aromatic CompoundsSynthesis, Reactivity, and Physical Properties
inferredcites →https://doi.org/10.1021/cr0505425openalex-snapshot
Topology in Chemistry: Designing Möbius Molecules
inferredcites →https://doi.org/10.1021/cr400088wopenalex-snapshot
Subphthalocyanines, Subporphyrazines, and Subporphyrins: Singular Nonplanar Aromatic Systems
inferredcites →https://doi.org/10.1021/ic010394aopenalex-snapshot
Palladium(II) Complexes of Oxybenziporphyrin
inferredcites →https://doi.org/10.1021/ic061091popenalex-snapshot
Cadmium(II) and Zinc(II) Complexes ofS-Confused Thiaporphyrin
inferredcites →https://doi.org/10.1021/ic2027175openalex-snapshot
Nickel(II) and Palladium(II) Thiaethyneporphyrins. Intramolecular Metal(II)−η2-CC Interaction inside a Porphyrinoid Frame
inferredcites →https://doi.org/10.1021/ic701248uopenalex-snapshot
Germanium Phthalocyanine, GePc, and the Reduced Complexes SiPc(pyridine)2 and GePc(pyridine)2 Containing Antiaromatic π-Electron Circuits
inferredcites →https://doi.org/10.1021/ic8004147openalex-snapshot
Heterobismetal Complexes of [26]Hexaphyrin(1.1.1.1.1.1)
inferredcites →https://doi.org/10.1021/ja00973a009openalex-snapshot
Induced Paramagnetic Ring Currents
inferredcites →https://doi.org/10.1021/ja051662xopenalex-snapshot
Aromatic and Antiaromatic Gold(III) Hexaphyrins with Multiple Gold−Carbon Bonds
inferredcites →https://doi.org/10.1021/ja052842+openalex-snapshot
Synthesis and Structure of 16 π Octaalkyltetraphenylporphyrins
inferredcites →https://doi.org/10.1021/ja053723xopenalex-snapshot
Dithiadiazuliporphyrin: Facile Generation of Carbaporphyrinoid Cation Radical and Dication
inferredcites →https://doi.org/10.1021/ja0544713openalex-snapshot
An Antiaromatic Porphyrin Complex: Tetraphenylporphyrinato(silicon)(L)2 (L = THF or Pyridine)
inferredcites →https://doi.org/10.1021/ja069324zopenalex-snapshot
meso-Aryl-Substituted Subporphyrins: Synthesis, Structures, and Large Substituent Effects on Their Electronic Properties
inferredcites →https://doi.org/10.1021/ja070794iopenalex-snapshot
Reversible Oxidation State Change in Germanium(tetraphenylporphyrin) Induced by a Dative Ligand: Aromatic GeII(TPP) and Antiaromatic GeIV(TPP)(pyridine)2
inferredcites →https://doi.org/10.1021/ja0712120openalex-snapshot
Synthesis and Characterization of meso-Triarylsubporphyrins
inferredcites →https://doi.org/10.1021/ja0744908openalex-snapshot
Peripheral Fabrications of a Bis-Gold(III) Complex of [26]Hexaphyrin(1.1.1.1.1.1) and Aromatic versus Antiaromatic Effect on Two-Photon Absorption Cross Section
inferredcites →https://doi.org/10.1021/ja205738zopenalex-snapshot
A Porphyrin with a C═C Unit at Its Center
inferredcites →https://doi.org/10.1021/ja710664yopenalex-snapshot
Planar Meso Pentafluorophenyl Core Modified Isophlorins
inferredcites →https://doi.org/10.1021/ja711039copenalex-snapshot
Palladium Vacataporphyrin Reveals Conformational Rearrangements Involving Hückel and Möbius Macrocyclic Topologies
inferredcites →https://doi.org/10.1021/ja801983dopenalex-snapshot
Unambiguous Identification of Möbius Aromaticity formeso-Aryl-Substituted [28]Hexaphyrins(1.1.1.1.1.1)
inferredcites →https://doi.org/10.1021/ja8068769openalex-snapshot
A Facile One-Pot Synthesis of meso-Aryl-Substituted [14]Triphyrin(2.1.1)
inferredcites →https://doi.org/10.1021/ja909913yopenalex-snapshot
Three-Level Topology Switching in a Molecular Möbius Band
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/jo00105a025openalex-snapshot
A Simple Route to Sulfur Bridged Annulenes
inferredcites →https://doi.org/10.1021/jo025773fopenalex-snapshot
5,10,15-Triaryl-21,23-dioxacorrole and Its Isomer with a Protruding Furan Ring
inferredcites →https://doi.org/10.1021/jo026748copenalex-snapshot
Contracted and Expandedmeso-Alkynyl Porphyrinoids: from Triphyrin to Hexaphyrin
inferredcites →https://doi.org/10.1021/jo0623437openalex-snapshot
22-Hydroxybenziporphyrin: Switching of Antiaromaticity by Phenol−Keto Tautomerization
inferredcites →https://doi.org/10.1021/jo7015218openalex-snapshot
Dioxadiazuliporphyrin: A Near-IR Redox Switchable Chromophore
inferredcites →https://doi.org/10.1021/jo902060bopenalex-snapshot
Synthesis and Reactions of Phosphaporphyrins: Reconstruction of π-Skeleton Triggered by Oxygenation of a Core Phosphorus Atom
inferredcites →https://doi.org/10.1021/jz1017366openalex-snapshot
Origin of Ultrafast Radiationless Deactivation Dynamics of Free-Base Subpyriporphyrins
inferredcites →https://doi.org/10.1021/ol0363265openalex-snapshot
Carbaporphyrinoid Chemistry Has a Silver Lining! Silver(III) Oxybenzi-, Oxynaphthi-, Tropi-, and Benzocarbaporphyrins
inferredcites →https://doi.org/10.1021/ol060772lopenalex-snapshot
The Doubly Oxidized, Antiaromatic Tetraphenylporphyrin Complex [Li(TPP)][BF4]
inferredcites →https://doi.org/10.1021/ol7029118openalex-snapshot
Monophosphaporphyrins: Oxidative π-Extension at the Peripherally Fused Carbocycle of the Phosphaporphyrin Ring
inferredcites →https://doi.org/10.1038/nature02224openalex-snapshot
Synthesis of a Möbius aromatic hydrocarbon
inferredcites →https://doi.org/10.1039/a702215hopenalex-snapshot
Protonation of 5,10,15,20-tetraphenylsapphyrin—identification of inverted and planar dicationic forms
inferredcites →https://doi.org/10.1039/b311178dopenalex-snapshot
Assessment of aromaticity via molecular response properties
inferredcites →https://doi.org/10.1039/b605984hopenalex-snapshot
Dithiaethyneazuliporphyrin - a contracted heterocarbaporphyrin
inferredcites →https://doi.org/10.1039/c2sc21791kopenalex-snapshot
2,3,17,18-Tetraethylsulfanyl [30]hexaphyrin(1.1.1.1.1.1) as the first aromatic isophlorin-type free-base
inferredcites →https://doi.org/10.1039/j39710003681openalex-snapshot
Synthesis of porphin analogues containing furan and/or thiophen rings
inferredcites →https://doi.org/10.1071/ch9661221openalex-snapshot
The synthesis of [18]annulene trioxide
inferredcites →https://doi.org/10.1142/s1088424611004063openalex-snapshot
Origin of aromatic character in porphyrinoid systems
inferredcites →https://doi.org/10.1351/pac199365010143openalex-snapshot
The porphyrins from the 'annulene chemist's' perspective
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.12688/openreseurope.19690.1zenodo-depositor-declared
Concealed antiaromaticity
inferred← citeshttps://doi.org/10.1002/9781119085928.ch2openalex-snapshot
Simple Electron Counting Rules
inferred← citeshttps://doi.org/10.1002/advs.202416223openalex-snapshot
Pyridine‐Fused Bis(azacorrole)s: Easily Accessible NIR III Absorbing Cation Radicals and Biradicaloids of Antiaromatic Ground State
inferred← citeshttps://doi.org/10.1002/ajoc.202200556openalex-snapshot
Pd II and Ni II Complexes of Earring Porphyrins with Distorted Coordination Geometries
inferred← citeshttps://doi.org/10.1002/ange.201508009openalex-snapshot
Hexaphyrin–Cyclodextrin Hybrids: A Nest for Switchable Aromaticity, Asymmetric Confinement, and Isomorphic Fluxionality
inferred← citeshttps://doi.org/10.1002/ange.201508033openalex-snapshot
A Rhodium‐Mediated Contraction of Benzene to Cyclopentadiene: Transformations of Rhodium(III) m‐Benziporphyrin
inferred← citeshttps://doi.org/10.1002/ange.201602083openalex-snapshot
Aromaticity Reversal in the Lowest Excited Triplet State of Archetypical Möbius Heteroannulenic Systems
inferred← citeshttps://doi.org/10.1002/ange.201709859openalex-snapshot
meso‐Aryl [20]π Homoporphyrin: The Simplest Expanded Porphyrin with the Smallest Möbius Topology
inferred← citeshttps://doi.org/10.1002/ange.201801555openalex-snapshot
The Curious Case of a Parasitic Twin of the Corroles
inferred← citeshttps://doi.org/10.1002/ange.201904819openalex-snapshot
Organoboron Complexes in Edge‐Sharing Macrocycles: The Triphyrin(2.1.1)–Tetraphyrin(1.1.1.1) Hybrid
inferred← citeshttps://doi.org/10.1002/ange.202011848openalex-snapshot
(Aza)Acenes Share the C2 Bridge with (Anti)Aromatic Macrocycles: Local vs. Global Delocalization Paths
inferred← citeshttps://doi.org/10.1002/ange.202300437openalex-snapshot
Easily Switchable 18π‐, 19π‐, and 20π‐Conjugation of Diazaporphyrin Double‐Pincer Bispalladium Complexes
inferred← citeshttps://doi.org/10.1002/ange.202400780openalex-snapshot
Breaking Global Diatropic Current to Tame Diradicaloid Character: Thiele's Hydrocarbon Under Macrocyclic Constraints
inferred← citeshttps://doi.org/10.1002/anie.201508009openalex-snapshot
Hexaphyrin–Cyclodextrin Hybrids: A Nest for Switchable Aromaticity, Asymmetric Confinement, and Isomorphic Fluxionality
inferred← citeshttps://doi.org/10.1002/anie.201508033openalex-snapshot
A Rhodium‐Mediated Contraction of Benzene to Cyclopentadiene: Transformations of Rhodium(III) m‐Benziporphyrin
inferred← citeshttps://doi.org/10.1002/anie.201602083openalex-snapshot
Aromaticity Reversal in the Lowest Excited Triplet State of Archetypical Möbius Heteroannulenic Systems
inferred← citeshttps://doi.org/10.1002/anie.201709859openalex-snapshot
meso‐Aryl [20]π Homoporphyrin: The Simplest Expanded Porphyrin with the Smallest Möbius Topology
inferred← citeshttps://doi.org/10.1002/anie.201801555openalex-snapshot
The Curious Case of a Parasitic Twin of the Corroles
inferred← citeshttps://doi.org/10.1002/anie.201904819openalex-snapshot
Organoboron Complexes in Edge‐Sharing Macrocycles: The Triphyrin(2.1.1)–Tetraphyrin(1.1.1.1) Hybrid
inferred← citeshttps://doi.org/10.1002/anie.202011848openalex-snapshot
(Aza)Acenes Share the C2 Bridge with (Anti)Aromatic Macrocycles: Local vs. Global Delocalization Paths
inferred← citeshttps://doi.org/10.1002/anie.202300437openalex-snapshot
Easily Switchable 18π‐, 19π‐, and 20π‐Conjugation of Diazaporphyrin Double‐Pincer Bispalladium Complexes
inferred← citeshttps://doi.org/10.1002/anie.202400780openalex-snapshot
Breaking Global Diatropic Current to Tame Diradicaloid Character: Thiele's Hydrocarbon Under Macrocyclic Constraints
inferred← citeshttps://doi.org/10.1002/asia.201600177openalex-snapshot
Phenylene‐Bridged Core‐Modified Planar Aromatic Octaphyrin: Aromaticity, Photophysical and Anion Receptor Properties
inferred← citeshttps://doi.org/10.1002/asia.201901422openalex-snapshot
Multi‐Cation Coordination in Porphyrinoids
inferred← citeshttps://doi.org/10.1002/asia.202101141openalex-snapshot
Synthesis and Structural Properties of NIR‐Absorbing Pyridine‐Containing Heptaphyrins
inferred← citeshttps://doi.org/10.1002/celc.202100063openalex-snapshot
Electrochemical Characterization of Bis‐Cobalt Hexaphyrin: A Selective Electrocatalyst for the Two‐Electron Reduction of Oxygen in Acid Media
inferred← citeshttps://doi.org/10.1002/chem.201505116openalex-snapshot
[32]π Fused Core‐Modified Heptaphyrin with Möbius Aromaticity
inferred← citeshttps://doi.org/10.1002/chem.201604458openalex-snapshot
Gold(III) Triggered Transformations of 22‐Methyl‐m‐benziporphyrin Involving an Effective Contraction of Benzene to Cyclopentadiene
inferred← citeshttps://doi.org/10.1002/chem.201704411openalex-snapshot
Rhodium‐Induced Reversible C−C Bond Cleavage: Transformations of Rhodium(III) 22‐Alkyl‐m‐benziporphyrins
inferred← citeshttps://doi.org/10.1002/chem.201800854openalex-snapshot
A 1,5‐Naphthyridine‐Fused Porphyrin Dimer: Intense NIR Absorption and Facile Redox Interconversion with Its Reduced Congener
inferred← citeshttps://doi.org/10.1002/chem.201804983openalex-snapshot
Three‐Stage Aromaticity Switching in Boron(III) and Phosphorus(V) N‐Fused p‐Benziporphyrin
inferred← citeshttps://doi.org/10.1002/chem.201903215openalex-snapshot
C−H and C−M Activation, Aromaticity Tuning, and Co⋅⋅⋅Ru Interactions Confined in the Azuliporphyrin Framework
inferred← citeshttps://doi.org/10.1002/chem.201903269openalex-snapshot
Phosphole‐Fused Dehydropurpurins via Titanium‐Mediated [2+2+1] Cyclization Strategy
inferred← citeshttps://doi.org/10.1002/chem.201903863openalex-snapshot
Aromatic and Antiaromatic Pathways in Triphyrin(2.1.1) Annelated with Benzo[b]heterocycles
inferred← citeshttps://doi.org/10.1002/chem.201904036openalex-snapshot
C−H and C−M Activation, Aromaticity Tuning, and Co⋅⋅⋅Ru Interactions Confined in the Azuliporphyrin Framework
inferred← citeshttps://doi.org/10.1002/chem.201905823openalex-snapshot
Facile Redox‐Induced Aromatic–Antiaromatic Interconversion of a β‐Tetracyano‐21,23‐Dithiaporphyrin under Ambient Conditions
inferred← citeshttps://doi.org/10.1002/chem.202100944openalex-snapshot
5,11‐Diazadibenzo[hi,qr]tetracene: Synthesis, Properties, and Reactivity toward Nucleophilic Reagents
inferred← citeshttps://doi.org/10.1002/chem.202400812openalex-snapshot
Stabilization of the Neutral [25]Hexaphyrin(1.0.1.0.1.0) Radical by Hetero‐Bimetal‐Coordination
inferred← citeshttps://doi.org/10.1002/chem.202501085openalex-snapshot
Bis(10‐oxacorrole) with Fused Pyridine as a Linker: Synthesis, Structure, and Interaction between the Subunits in the Neutral, Mono‐, and Dicationic States
inferred← citeshttps://doi.org/10.1002/chin.201542231openalex-snapshot
ChemInform Abstract: Aromaticity Switching in Porphyrinoids
inferred← citeshttps://doi.org/10.1002/cplu.201900068openalex-snapshot
Regioselective Oxidative Ring Cleavage of Antiaromatic Nickel(II) Norcorrole to Dialkoxybis(dipyrrin)s
inferred← citeshttps://doi.org/10.1002/cplu.202400636openalex-snapshot
Conjugation Paths in Oxatriphyrin(2.1.1) – C2 Bridge Modifications
inferred← citeshttps://doi.org/10.1002/ejoc.202200564openalex-snapshot
7,12‐Dihydrobenzo[de]indolo[3,2‐b]quinoline: Unique Reactivity and Redox Interconversion
inferred← citeshttps://doi.org/10.1002/ejoc.202300870openalex-snapshot
28π Non‐Fused Hexaphyrin: Synthesis, Protonation Triggered Möbius Aromaticity and Structural Properties
inferred← citeshttps://doi.org/10.1002/ejoc.70590openalex-snapshot
Synthesis and Properties of Unusually Stable Antiaromatic Porphyrinoids
inferred← citeshttps://doi.org/10.1002/jms.3760openalex-snapshot
ESI‐MS/MS of expanded porphyrins: a look into their structure and aromaticity
inferred← citeshttps://doi.org/10.1002/poc.4127openalex-snapshot
A study on the aromaticity and conjugation pathways of diheterodiazuliporphyrins and their dications
inferred← citeshttps://doi.org/10.1007/s12668-017-0424-0openalex-snapshot
Nanostructured Stable Floating М-Mono- and Bilayers and Langmuir-Schaefer Films of 5,10,15-Triphenylcorrole
inferred← citeshttps://doi.org/10.1016/bs.aihch.2017.02.001openalex-snapshot
The Literature of Heterocyclic Chemistry, Part XV, 2015
inferred← citeshttps://doi.org/10.1016/j.ccr.2019.213172openalex-snapshot
Synthesis, properties and coordination chemistry of [14]triphyrins(2.1.1)
inferred← citeshttps://doi.org/10.1021/acs.accounts.6c00503openalex-snapshot
Norcorrole: A Stable Porphyrinoid for Exploration of Antiaromaticity
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00326openalex-snapshot
Carbaporphyrinoid Systems
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00345openalex-snapshot
Porphycenes and Related Isomers: Synthetic Aspects
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00371openalex-snapshot
Chemistry of meso -Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00403openalex-snapshot
Recent Advances in Subporphyrins and Triphyrin Analogues: Contracted Porphyrins Comprising Three Pyrrole Rings
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00335openalex-snapshot
Porphyrin–Amino Acid Conjugates
inferred← citeshttps://doi.org/10.1021/acs.joc.5b01348openalex-snapshot
5,20-Di(pyridin-2-yl)-[28]hexaphyrin(1.1.1.1.1.1): A Stable Hückel Antiaromatic Hexaphyrin Stabilized by Intramolecular Hydrogen Bonding and Protonation-Induced Conformational Twist To Gain Möbius Aromaticity
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01812openalex-snapshot
Dibenzidecaphyrins (1.0.0.1.1.1.0.0.1.1) and Their Bis-BF2 Complexes
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01047openalex-snapshot
Reductive Dimerization of Macrocycles Activated by BBr3
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03605openalex-snapshot
Edge Decoration of Anthracene Switches Global Diatropic Current That Controls the Acene Reactivity
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01625openalex-snapshot
Diagnosing Ring Current(s) in Figure-Eight Skeletons: A 3D Through-Space Conjugation in the Two-Loops Crossing
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c02968openalex-snapshot
Meso-Engineered Carbaporphyrin Dimers with Nonaromatic and Antiaromatic Properties
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c03188openalex-snapshot
Global Antiaromaticity Induced by Installation of 3,5-Di(pyrrol-2-yl)BODIPY across the meso Position of Porphyrinoids
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03805openalex-snapshot
Protonation-Triggered Hückel and Möbius Aromatic Transformations in Nonaromatic Core-Modified [30]Hexaphyrin(2.1.1.2.1.1) and Annulated [28]Hexaphyrin(2.1.1.0.1.1)
inferred← citeshttps://doi.org/10.1021/jacs.1c00476openalex-snapshot
meso-Oxoisocorroles: Tunable Antiaromaticity by Metalation and Coordination of Lewis Acids as Well as Aromaticity Reversal in the Triplet Excited State
inferred← citeshttps://doi.org/10.1021/jacs.1c11716openalex-snapshot
Highly Stable Neutral Corrole Radical: Amphoteric Aromatic–Antiaromatic Switching and Efficient Photothermal Conversion
inferred← citeshttps://doi.org/10.1021/jacs.3c00942openalex-snapshot
Isolation, Reactivity, and Tunable Properties of a Strained Antiaromatic Osmacycle
inferred← citeshttps://doi.org/10.1021/jacs.5c01135openalex-snapshot
Iso-dibenzo[ g , p ]chrysene-Fused Bis-dicarbaporphyrin: Pd Coordination-Induced Global Aromaticity and Stabilization of Double In-Plane Pd(IV) Cations
inferred← citeshttps://doi.org/10.1021/jacs.5c18822openalex-snapshot
Expanded Boraporphyrinoids: Boron Macrocycles with Redox Switchable Magnetic (Anti)aromaticity and Strong Near-Infrared Absorption
inferred← citeshttps://doi.org/10.1021/jacs.8b07973openalex-snapshot
meso -Triaryl-Substituted Smaragdyrins: Facile Aromaticity Switching
inferred← citeshttps://doi.org/10.1021/jacs.8b12899openalex-snapshot
Switchable Aromaticity in an Isostructural Mn Phthalocyanine Series Isolated in Five Separate Redox States
inferred← citeshttps://doi.org/10.1021/jacs.9b01357openalex-snapshot
Diphenanthrioctaphyrin(1.1.1.0.1.1.1.0): Conformational Switching Controls the Stereochemical Dynamics of the Topologically Chiral System
inferred← citeshttps://doi.org/10.1038/s41467-020-20072-9openalex-snapshot
Benzene- and pyridine-incorporated octaphyrins with different coordination modes toward two PdII centers
inferred← citeshttps://doi.org/10.1038/s41467-025-56892-wopenalex-snapshot
A fully conjugated meso-boron-substituted porphyrinoid combining Lewis acidity with redox-switchable aromaticity
inferred← citeshttps://doi.org/10.1038/s41598-019-39972-yopenalex-snapshot
Norcorrole as a Delocalized, Antiaromatic System
inferred← citeshttps://doi.org/10.1039/c7qm00176bopenalex-snapshot
Direct amination of the antiaromatic Ni II norcorrole
inferred← citeshttps://doi.org/10.1039/c8qo00751aopenalex-snapshot
Aromaticity control via modifications of a macrocyclic frame: 5,6-dimethoxyphenanthriporphyrin and 5,6-dioxophenanthriporphyrin
inferred← citeshttps://doi.org/10.1039/c8sc02448kopenalex-snapshot
Reversible π-system switching of thiophene-fused thiahexaphyrins by solvent and oxidation/reduction
inferred← citeshttps://doi.org/10.1039/c9cc01201jopenalex-snapshot
A route to a cyclobutane-linked double-looped system via a helical macrocycle
inferred← citeshttps://doi.org/10.1039/c9cc08877fopenalex-snapshot
Rhenium( i ) sapphyrins: remarkable difference between the C 6 F 5 and CF 3 -substituted derivatives
inferred← citeshttps://doi.org/10.1039/c9cp06120gopenalex-snapshot
Switching between Hückel and Möbius aromaticity: a density functional theory and information-theoretic approach study
inferred← citeshttps://doi.org/10.1039/c9ob00489kopenalex-snapshot
Acid–base controlled multiple conformation and aromaticity switches in tren-capped hexaphyrins
inferred← citeshttps://doi.org/10.1039/c9qo00294dopenalex-snapshot
A controlled blue-shift in meso -nitrogen aryl fused DIPY and BODIPY skeletons
inferred← citeshttps://doi.org/10.1039/d0cp04815aopenalex-snapshot
Monitoring aromatic ring-currents in Mg-porphyrin by time-resolved circular dichroism
inferred← citeshttps://doi.org/10.1039/d0qo00436gopenalex-snapshot
An exocyclic π-system extension of the phenanthriporphyrin framework: towards azaaceneporphyrinoids
inferred← citeshttps://doi.org/10.1039/d1cs00666eopenalex-snapshot
Inverted and fused expanded heteroporphyrins
inferred← citeshttps://doi.org/10.1039/d2cc06648copenalex-snapshot
Oxidative insertion of amines into conjugated macrocycles: transformation of antiaromatic norcorrole into aromatic azacorrole
inferred← citeshttps://doi.org/10.1039/d2cs00784copenalex-snapshot
Organometallic chemistry confined within a porphyrin-like framework
inferred← citeshttps://doi.org/10.1039/d2qo00437bopenalex-snapshot
Phenanthrene cyclocarbonylation – core post-synthetic modification of phenanthriporphyrin
inferred← citeshttps://doi.org/10.1039/d2qo00960aopenalex-snapshot
21-Carba-23-oxaporphyrinoids and 21-oxo-21-carba-23-oxaporphyrinoids: macrocyclic π-conjugation involving the carbonyl moiety
inferred← citeshttps://doi.org/10.1039/d4qi00684dopenalex-snapshot
Strain-based design, direct macrocyclization, and metal complexation of thiazole-containing calix[3]pyrrole analogues
inferred← citeshttps://doi.org/10.1039/d4qo01566eopenalex-snapshot
Folding of a dynamic macrocyclic system to stabilize its cation radical state
inferred← citeshttps://doi.org/10.1039/d5dt00221dopenalex-snapshot
Synthesis, structure, and properties of antiaromatic P V O complexes of triphyrins(2.1.1)
inferred← citeshttps://doi.org/10.1039/d6ra00486eopenalex-snapshot
Theoretical study on the geometry, aromaticity and electronic properties of porphyrin analogues
inferred← citeshttps://doi.org/10.1055/s-0039-1690748openalex-snapshot
Multiple Coordination in Porphyrinoid Hybrid: Changing the Delocalization within the Extended π-System
inferred← citeshttps://doi.org/10.1142/s108842461750016xopenalex-snapshot
Electrochemistry and spectroelectrochemistry of metallohexaphyrins containing bis-copper or bis-zinc central metal ions
inferred← citeshttps://doi.org/10.1142/s1088424619501074openalex-snapshot
Meso-1,4-phenylene bridged nickel norcorrole dimer
inferred← citeshttps://doi.org/10.1142/s1088424621501248openalex-snapshot
One-pot reaction of aminoarenes and porphyrin – A fused amino acid-tetraphyrin(1.1.1.1) hybrid
inferred← citeshttps://doi.org/10.1515/psr-2019-0081openalex-snapshot
Changes in porphyrin’s conjugation based on synthetic and post-synthetic modifications
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