On the public citation graph
Rothemund and Adler-Longo reactions revisited: synthesis of tetraphenylporphyrins under equilibrium conditions
0 signed · 1446 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4689530openalex-extracted
Exploring the Effect of Tetraphenyl Porphyrin Chemical Structure on the Performance of Polymer-Based Pressure-Sensitive Paints
inferred← citeshttps://doi.org/10.2139/ssrn.4750256openalex-extracted
Porphyrin Photosensitizer Molecules as Effective Medicine Candidates for Photodynamic Therapy: Electronic Structure Information Aided Design
inferred← citeshttps://doi.org/10.1002/(sici)1097-0215(19960927)68:1<114::aid-ijc20>3.0.co;2-aopenalex-snapshot
Synthesis of a nickel tetracarboranylphenylporphyrin for boron neutron-capture therapy: Biodistribution and toxicity in tumor-bearing mice
inferred← citeshttps://doi.org/10.1002/(sici)1097-0290(199821)61:2<107::aid-bit5>3.0.co;2-qopenalex-snapshot
Are porphyrin mixtures favorable photodynamic anticancer drugs? A model study with combinatorial libraries of tetraphenylporphyrins
inferred← citeshttps://doi.org/10.1002/(sici)1097-458x(200002)38:2<67::aid-mrc604>3.0.co;2-jopenalex-snapshot
EPR and ENDOR of radicals of chlorin- and bacteriochlorin-quinone model compounds for electron transfer in photosynthesis
inferred← citeshttps://doi.org/10.1002/(sici)1097-4601(2000)32:5<271::aid-kin2>3.0.co;2-#openalex-snapshot
Structural stabilities of water‐soluble MnTDCSPP, MnTSPP, and supported analogues toward hydrogen peroxide and sodium hypochlorite
inferred← citeshttps://doi.org/10.1002/(sici)1099-0682(199801)1998:1<1::aid-ejic1>3.0.co;2-#openalex-snapshot
Construction of One‐Dimensional Multicomponent Molecular Arrays: Control of Electronic and Molecular Motions
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(199907)1999:7<1527::aid-ejoc1527>3.0.co;2-fopenalex-snapshot
Synthesis and Mesogenic Properties of Porphyrin Octaesters
inferred← citeshttps://doi.org/10.1002/(sici)1099-0690(200002)2000:4<583::aid-ejoc583>3.0.co;2-eopenalex-snapshot
D2-Symmetric Chiroporphyrins Derived from (1R)-cis-Hemicaronaldehydic Acid: Preparation and Spectral Characterization
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(199801/02)2:1<69::aid-jpp55>3.0.co;2-1openalex-snapshot
Spectroscopic and Electrochemical Studies on Oxaporphyrins and Oxathiaporphyrins
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(199807/10)2:4/5<315::aid-jpp73>3.0.co;2-lopenalex-snapshot
Energy Transfer in a Supramolecular Complex Assembled via Sapphyrin Dimer-mediated Dicarboxylate Anion Chelation
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(199811/12)2:6<455::aid-jpp67>3.0.co;2-copenalex-snapshot
Novel and Improved Syntheses of 5,15-Diphenylporphyrin and its Dipyrrolic Precursors
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(199811/12)2:6<501::aid-jpp89>3.0.co;2-mopenalex-snapshot
Synthesis and Characterization of meso-Tetraphenylporphyrin-Corrole Unsymmetrical Dyads
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(199811/12)2:6<511::aid-jpp102>3.0.co;2-eopenalex-snapshot
A Convenient Procedure for Moderate-scale Rothemund Synthesis of Lipophilic Porphyrins: an Alternative to the Adler–Longo and Lindsey Methodologies
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(199902)3:2<117::aid-jpp110>3.0.co;2-xopenalex-snapshot
Ground and Excited State Electronic Properties of Halogenated Tetraarylporphyrins: Tuning the Building Blocks for Porphyrin-based Photonic Devices
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(199902)3:2<99::aid-jpp109>3.0.co;2-6openalex-snapshot
Synthesis, Reactivity and Structural Chemistry of 5,10,15,20-Tetraalkylporphyrins
inferred← citeshttps://doi.org/10.1002/(sici)1099-1409(200006/07)4:4<319::aid-jpp246>3.0.co;2-2openalex-snapshot
Syntheses and chemistry of porphyrins
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19980703)110:13/14<2037::aid-ange2037>3.0.co;2-vopenalex-snapshot
Ein Tetraphenylporphyrin mit vier Fullerensubstituenten
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981102)110:21<3172::aid-ange3172>3.0.co;2-5openalex-snapshot
Windmühlenartige Porphyrinaggregate als lichtsammelnde Antennenkomplexe
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19981102)110:21<3176::aid-ange3176>3.0.co;2-iopenalex-snapshot
Supramolekulare Aggregate heterogener Multiporphyrinanordnungen – die Strukturen von [{ZnII(tpp)}2(tpyp)] und dem Koordinationspolymer [{[MnIII(tpp)]2(tpyp)(ClO4)2}]
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(19991216)111:24<3866::aid-ange3866>3.0.co;2-ropenalex-snapshot
Cyclooctapyrrole mit 8er-Konformation: Enantiomerentrennung und Bestimmung der absoluten Konfiguration eines zweikernigen Metallkomplexes
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000403)112:7<1344::aid-ange1344>3.0.co;2-8openalex-snapshot
Crystal Engineering of Metalloporphyrin Zeolite Analogues
inferred← citeshttps://doi.org/10.1002/(sici)1521-3757(20000403)112:7<1348::aid-ange1348>3.0.co;2-lopenalex-snapshot
Charge Separation in a Molecular Triad Consisting of an Iridium(III) – bis-terpy Central Core and Porphyrins as Terminal Electron Donor and Acceptor Groups
inferred← citeshttps://doi.org/10.1002/(sici)1521-3773(20000403)39:7<1292::aid-anie1292>3.0.co;2-vopenalex-snapshot
Charge Separation in a Molecular Triad Consisting of an Iridium(III) – bis-terpy Central Core and Porphyrins as Terminal Electron Donor and Acceptor Groups
inferred← citeshttps://doi.org/10.1002/0471264180.os070.09openalex-snapshot
3,4‐Diethylpyrrole and 2,3,7,8,12,13,17,18‐Octaethylporphyrin
inferred← citeshttps://doi.org/10.1002/1099-0690(200004)2000:7<1165::aid-ejoc1165>3.0.co;2-8openalex-snapshot
Chiral Atropisomeric Metalloporphyrins in the Enantioselective Styrene Epoxidation
inferred← citeshttps://doi.org/10.1002/1099-0690(200006)2000:12<2303::aid-ejoc2303>3.0.co;2-uopenalex-snapshot
Porphyrin-o-quinones as Model Systems for Electron Transfer and Catecholase Reactions
inferred← citeshttps://doi.org/10.1002/1099-0690(200012)2000:24<4047::aid-ejoc4047>3.0.co;2-8openalex-snapshot
Self-Assembly by Hydrogen Bonding and π−π Interactions in the Crystal of a Porphyrin − Attempts to Mimic Bacteriochlorophyllc
inferred← citeshttps://doi.org/10.1002/1099-0690(200101)2001:1<181::aid-ejoc181>3.0.co;2-3openalex-snapshot
Fluorous Biphasic Catalytic Oxidation of Sulfides by Molecular Oxygen/2,2-Dimethylpropanal
inferred← citeshttps://doi.org/10.1002/1099-1395(200007)13:7<382::aid-poc266>3.0.co;2-5openalex-snapshot
Solid-state supramolecular chemistry of porphyrins. Hydrogen-bonded networks and porous crystals ofmeso-tetra[4-(3,5-diaminotriazino)phenyl]porphyrin
inferred← citeshttps://doi.org/10.1002/1099-1409(200011)4:7<659::aid-jpp259>3.0.co;2-kopenalex-snapshot
Dendritic porphyrins: synthesis and third-order optical non-linearity
inferred← citeshttps://doi.org/10.1002/1521-3757(20010105)113:1<76::aid-ange76>3.0.co;2-fopenalex-snapshot
Dendritisch eingeschlossene aktive Zentren: Anwendung des Isolationsprinzips der Natur in der Biomimetik und den Materialwissenschaften
inferred← citeshttps://doi.org/10.1002/1521-3757(20020315)114:6<938::aid-ange938>3.0.co;2-kopenalex-snapshot
Dynamische kovalente Chemie
inferred← citeshttps://doi.org/10.1002/1521-3765(20020201)8:3<655::aid-chem655>3.0.co;2-dopenalex-snapshot
1,1′-Binaphthyl-Substituted Macrocycles as Receptors for Saccharide Recognition
inferred← citeshttps://doi.org/10.1002/1521-3773(20010105)40:1<74::aid-anie74>3.0.co;2-copenalex-snapshot
Dendritic Encapsulation of Function: Applying Nature's Site Isolation Principle from Biomimetics to Materials Science
inferred← citeshttps://doi.org/10.1002/1521-3773(20020315)41:6<898::aid-anie898>3.0.co;2-eopenalex-snapshot
Dynamic Covalent Chemistry
inferred← citeshttps://doi.org/10.1002/9780470661345.smc171openalex-snapshot
Porphyrinoids: Highly Versatile, Redox‐Active Scaffolds for Supramolecular Design and Biomimetic Applications
inferred← citeshttps://doi.org/10.1002/9780470682531.pat1020openalex-snapshot
Multiporphyrinic Arrays Containing Hydroporphyrins
inferred← citeshttps://doi.org/10.1002/9780470745533.ch1openalex-snapshot
Functional Oligothiophene‐Based Materials: Nanoarchitectures and Applications
inferred← citeshttps://doi.org/10.1002/9781118778173.ch15openalex-snapshot
Cycloreversion Approach For Preparation of Large π‐Conjugated Compounds
inferred← citeshttps://doi.org/10.1002/9781119044123.ch2openalex-snapshot
The Fundamentals of Making Mechanical Bonds
inferred← citeshttps://doi.org/10.1002/9781119951438.eibc0104openalex-snapshot
Iron Porphyrin Chemistry
inferred← citeshttps://doi.org/10.1002/9783527637737.ch11openalex-snapshot
Five‐Membered Heterocycles with Two Heteroatoms: O and S Derivatives
inferred← citeshttps://doi.org/10.1002/9783527637737.ch26openalex-snapshot
Porphyrins: Syntheses and Reactions
inferred← citeshttps://doi.org/10.1002/9783527637737.ch4openalex-snapshot
Five‐Membered Heterocycles: Pyrrole and Related Systems
inferred← citeshttps://doi.org/10.1002/9783527652532.ch11openalex-snapshot
Synthesis of Pyrroles and Their Derivatives from Isocyanides
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz06077openalex-snapshot
dynamic covalent chemistry
inferred← citeshttps://doi.org/10.1002/9783527834204.ch18openalex-snapshot
2‐Aza‐21‐Carbaporphyrin in Construction of Chiral Supramolecular Assemblies
inferred← citeshttps://doi.org/10.1002/adma.19970090405openalex-snapshot
Mesogenic Zinc(u) complexes of 5,10,15,20‐ tetraarylethynyl‐substituted porphyrins
inferred← citeshttps://doi.org/10.1002/adma.200601850openalex-snapshot
Nonlinear Optical Properties of Porphyrins
inferred← citeshttps://doi.org/10.1002/adom.202303036openalex-snapshot
Metalloporphyrins as Building Blocks for Quantum Information Science
inferred← citeshttps://doi.org/10.1002/adsc.202400273openalex-snapshot
Suzuki‐Miyaura Reaction of Glycals with Base‐Labile Protecting Groups as a New Route to Glycoporphyrins
inferred← citeshttps://doi.org/10.1002/adsc.70300openalex-snapshot
A Scalable and Resource‐Saving Synthesis of Dipyrromethanes and Tetrapyrroles via Geminal Diethers: Minimal Polymer Formation and Facile Purification
inferred← citeshttps://doi.org/10.1002/ajoc.201900154openalex-snapshot
Acid Activation and Chemical Oxidation in the Synthesis of meso‐Tetraphenylporphyrin using a Mixed‐Solvent System
inferred← citeshttps://doi.org/10.1002/ange.1761051112openalex-snapshot
Octaethyltetraoxaporphyrin-Dikation – Pendant des Octaethylporphyrins in der Tetraoxaporphyrin-Reihe
inferred← citeshttps://doi.org/10.1002/ange.19901020306openalex-snapshot
Molekulare Erkennung mit konkaven Modellverbindungen
inferred← citeshttps://doi.org/10.1002/ange.19901021010openalex-snapshot
Phenylenverknüpfte, chinonsubstituierte Porphyrintrimere
inferred← citeshttps://doi.org/10.1002/ange.19931050218openalex-snapshot
Cobalttetra(hydrochinon)porphyrin als wirkungsvoller Elektronenüberträger bei der aeroben Pd‐katalysierten 1,4‐Diacetoxylierung von 1,3‐Cyclohexadien
inferred← citeshttps://doi.org/10.1002/ange.19941060212openalex-snapshot
Chiroporphyrine: ein Zugang zu asymmetrischen Porphyrinkatalysatoren mit stereogenen Zentren auf der Ringebene
inferred← citeshttps://doi.org/10.1002/ange.19941060721openalex-snapshot
Monoinvertiertes Tetra‐p‐tolylporphyrin: ein neues Porphyrinisomer
inferred← citeshttps://doi.org/10.1002/ange.19941061823openalex-snapshot
5, 10, 15, 20‐Tetra‐tert‐butylporphyrin und seine bemerkenswerte Reaktivität in 5, 15‐Stellung
inferred← citeshttps://doi.org/10.1002/ange.19941062220openalex-snapshot
Biomimetische Modelle für das photosynthetische Reaktionszentrum: ein kovalent mit einem redoxaktiven Kronenether verknüpftes Porphyrin
inferred← citeshttps://doi.org/10.1002/ange.19951070616openalex-snapshot
Tetraphenanthro[9,10‐b:9,10‐g:9,10‐l:9,10‐q]‐porphyrin, ein neues hochkonjugiertes Porphyrinderivat
inferred← citeshttps://doi.org/10.1002/ange.19951070804openalex-snapshot
Modellreaktionen für die Photosynthese – photoinduzierter Ladungs‐ und Energietransfer zwischen verknüpften Porphyrin‐ und Chinon‐Einheiten
inferred← citeshttps://doi.org/10.1002/ange.19971092308openalex-snapshot
Tetrathia‐ und Tetraoxarubyrine: aromatische, Gerüst‐modifizierte expandierte Porphyrine
inferred← citeshttps://doi.org/10.1002/ange.200201603openalex-snapshot
Die Eintopfkondensation von Pyrrolen mit Aldehyden als vielseitiger Selbstorganisationsprozess
inferred← citeshttps://doi.org/10.1002/ange.200503602openalex-snapshot
A Biomimetic Model for the Active Site of Iron‐Only Hydrogenases Covalently Bonded to a Porphyrin Photosensitizer
inferred← citeshttps://doi.org/10.1002/ange.200600892openalex-snapshot
A Quadruply Azulene‐Fused Porphyrin with Intense Near‐IR Absorption and a Large Two‐Photon Absorption Cross Section
inferred← citeshttps://doi.org/10.1002/ange.200604882openalex-snapshot
Synthesis of Calix[3]dipyrrins by a Modified Lindsey Protocol
inferred← citeshttps://doi.org/10.1002/ange.201002236openalex-snapshot
Homokonjugierte Push‐pull‐ und Spirosysteme: intramolekulare Charge‐Transfer‐Wechselwirkungen und nichtlineare optische Eigenschaften dritter Ordnung
inferred← citeshttps://doi.org/10.1002/ange.201207987openalex-snapshot
Antiaromatic Supramolecules: F⋅⋅⋅S, F⋅⋅⋅Se, and F⋅⋅⋅π Intermolecular Interactions in 32 π Expanded Isophlorins
inferred← citeshttps://doi.org/10.1002/ange.201402711openalex-snapshot
Durch Dithienylethen‐Einheiten modifizierte Rubyrine
inferred← citeshttps://doi.org/10.1002/ange.201407053openalex-snapshot
Superbenzol‐Porphyrin‐Konjugate
inferred← citeshttps://doi.org/10.1002/ange.201500732openalex-snapshot
Phenanthriporphyrin: An Antiaromatic Aceneporphyrinoid as a Ligand for a Hypervalent Organophosphorus(V) Moiety
inferred← citeshttps://doi.org/10.1002/ange.201503347openalex-snapshot
A 6,11,16‐Triarylbiphenylcorrole with an adj‐CCNN Core: Stabilization of an Organocopper(III) Complex
inferred← citeshttps://doi.org/10.1002/ange.201506847openalex-snapshot
Bright, “Clickable” Porphyrins for the Visualization of Oxygenation under Ambient Light
inferred← citeshttps://doi.org/10.1002/ange.201901808openalex-snapshot
A meso‐Tetraaryl‐21‐carbaporphyrin: Incorporation of a Cyclopentadiene Unit into a Porphyrin Architecture
inferred← citeshttps://doi.org/10.1002/ange.201907929openalex-snapshot
Konformativer Umbau von Porphyrinen als Rezeptoren mit schaltbaren N‐H⋅⋅⋅X‐Bindungsmodi
inferred← citeshttps://doi.org/10.1002/ange.201913024openalex-snapshot
On‐Surface Synthesis and Characterization of Triply Fused Porphyrin–Graphene Nanoribbon Hybrids
inferred← citeshttps://doi.org/10.1002/ange.202201327openalex-snapshot
Low‐Valent Zirconocene‐Mediated Synthesis of Porphyrin(2.1.2.1)s and Its Extension to Synthesis of a Porphyrin(2.1.2.1) Nanobarrel
inferred← citeshttps://doi.org/10.1002/ange.202208180openalex-snapshot
Porphyrinbasiertes organisches Netzwerk bestehend aus nachhaltigen Kohlenstoffpunkten für die Photopolymerisation
inferred← citeshttps://doi.org/10.1002/ange.202316431openalex-snapshot
Lichtinduzierte Polymerisation katalysiert durch Kohlenstoff‐Nanomaterialien
inferred← citeshttps://doi.org/10.1002/ange.202402915openalex-snapshot
Der Einschluss von nachhaltigen Kohlenstoffpunkten führt zu langnachleuchtenden Emittern und zu Photokatalysatoren für die radikalische Photopolymerisation
inferred← citeshttps://doi.org/10.1002/ange.202403754openalex-snapshot
Molecular Symmetry and Art: Visualizing the Near‐Symmetry of Molecules in Piet Mondrian's De Stijl
inferred← citeshttps://doi.org/10.1002/ange.202412978openalex-snapshot
Solution Versus On‐Surface Synthesis of Peripherally Oxygen‐Annulated Porphyrins through C−O Bond Formation
inferred← citeshttps://doi.org/10.1002/anie.199002451openalex-snapshot
Molecular Recognition with Model Systems
inferred← citeshttps://doi.org/10.1002/anie.199011341openalex-snapshot
Phenyl‐Linked Quinone‐Substituted Porphyrin Trimers
inferred← citeshttps://doi.org/10.1002/anie.199302631openalex-snapshot
Cobalt Tetra(hydroquinone)porphyrin: An Efficient Electron Transfer Reagent in Aerobic Pd‐Catalyzed 1,4‐Diacetoxylation of 1,3‐Cyclohexadiene
inferred← citeshttps://doi.org/10.1002/anie.199315971openalex-snapshot
Octaethyltetraoxaporphyrin Dication—Counterpart of Octaethylporphyrin in the Tetraoxaporphyrin Series
inferred← citeshttps://doi.org/10.1002/anie.199402201openalex-snapshot
Chiroporphyrins: An Approach to Asymmetric Catalysts with Stereocenters Near the Plane of the Porphyrin Ring
inferred← citeshttps://doi.org/10.1002/anie.199407791openalex-snapshot
Tetra‐p‐tolylporphyrin with an Inverted Pyrrole Ring: A Novel Isomer of Porphyrin
inferred← citeshttps://doi.org/10.1002/anie.199418791openalex-snapshot
5,10,15,20‐Tetra‐tert‐butylporphyrin and Its Remarkable Reactivity in the 5‐ and 15‐Positions
inferred← citeshttps://doi.org/10.1002/anie.199423181openalex-snapshot
Biomimetic Model for a Photosynthetic Reaction Center: A Porphyrin with a Covalently Linked, Redox‐Active Crown Ether
inferred← citeshttps://doi.org/10.1002/anie.199506831openalex-snapshot
Tetraphenanthro[9,10‐b:9,10‐g:9,10‐l:9,10‐q]‐porphyrin, a New Highly Conjugated Porphyrin System
inferred← citeshttps://doi.org/10.1002/anie.199508491openalex-snapshot
Model Reactions for Photosynthesis—Photoinduced Charge and Energy Transfer between Covalently Linked Porphyrin and Quinone Units
inferred← citeshttps://doi.org/10.1002/anie.199725981openalex-snapshot
Tetrathia‐ and Tetraoxarubyrins: Aromatic, Core‐Modified, Expanded Porphyrins
inferred← citeshttps://doi.org/10.1002/anie.200201603openalex-snapshot
A Perspective of One‐Pot Pyrrole–Aldehyde Condensations as Versatile Self‐Assembly Processes
inferred← citeshttps://doi.org/10.1002/anie.200503602openalex-snapshot
A Biomimetic Model for the Active Site of Iron‐Only Hydrogenases Covalently Bonded to a Porphyrin Photosensitizer
inferred← citeshttps://doi.org/10.1002/anie.200600892openalex-snapshot
A Quadruply Azulene‐Fused Porphyrin with Intense Near‐IR Absorption and a Large Two‐Photon Absorption Cross Section
inferred← citeshttps://doi.org/10.1002/anie.200604882openalex-snapshot
Synthesis of Calix[3]dipyrrins by a Modified Lindsey Protocol
inferred← citeshttps://doi.org/10.1002/anie.201002236openalex-snapshot
Homoconjugated Push–Pull and Spiro Systems: Intramolecular Charge‐Transfer Interactions and Third‐Order Optical Nonlinearities
inferred← citeshttps://doi.org/10.1002/anie.201207987openalex-snapshot
Antiaromatic Supramolecules: F⋅⋅⋅S, F⋅⋅⋅Se, and F⋅⋅⋅π Intermolecular Interactions in 32 π Expanded Isophlorins
inferred← citeshttps://doi.org/10.1002/anie.201402711openalex-snapshot
Core‐Modified Rubyrins Containing Dithienylethene Moieties
inferred← citeshttps://doi.org/10.1002/anie.201407053openalex-snapshot
Superbenzene–Porphyrin Conjugates
inferred← citeshttps://doi.org/10.1002/anie.201500732openalex-snapshot
Phenanthriporphyrin: An Antiaromatic Aceneporphyrinoid as a Ligand for a Hypervalent Organophosphorus(V) Moiety
inferred← citeshttps://doi.org/10.1002/anie.201503347openalex-snapshot
A 6,11,16‐Triarylbiphenylcorrole with an adj‐CCNN Core: Stabilization of an Organocopper(III) Complex
inferred← citeshttps://doi.org/10.1002/anie.201506847openalex-snapshot
Bright, “Clickable” Porphyrins for the Visualization of Oxygenation under Ambient Light
inferred← citeshttps://doi.org/10.1002/anie.201901808openalex-snapshot
A meso ‐Tetraaryl‐21‐carbaporphyrin: Incorporation of a Cyclopentadiene Unit into a Porphyrin Architecture
inferred← citeshttps://doi.org/10.1002/anie.201907929openalex-snapshot
Conformational Re‐engineering of Porphyrins as Receptors with Switchable N−H⋅⋅⋅X‐Type Binding Modes
inferred← citeshttps://doi.org/10.1002/anie.201913024openalex-snapshot
On‐Surface Synthesis and Characterization of Triply Fused Porphyrin–Graphene Nanoribbon Hybrids
inferred← citeshttps://doi.org/10.1002/anie.202201327openalex-snapshot
Low‐Valent Zirconocene‐Mediated Synthesis of Porphyrin(2.1.2.1)s and Its Extension to Synthesis of a Porphyrin(2.1.2.1) Nanobarrel
inferred← citeshttps://doi.org/10.1002/anie.202208180openalex-snapshot
A Porphyrin‐Based Organic Network Comprising Sustainable Carbon Dots for Photopolymerization
inferred← citeshttps://doi.org/10.1002/anie.202316431openalex-snapshot
Light‐Mediated Polymerization Catalyzed by Carbon Nanomaterials
inferred← citeshttps://doi.org/10.1002/anie.202402915openalex-snapshot
Confinement of Sustainable Carbon Dots Results in Long Afterglow Emitters and Photocatalyst for Radical Photopolymerization
inferred← citeshttps://doi.org/10.1002/anie.202403754openalex-snapshot
Molecular Symmetry and Art: Visualizing the Near‐Symmetry of Molecules in Piet Mondrian's De Stijl
inferred← citeshttps://doi.org/10.1002/anie.202412978openalex-snapshot
Solution Versus On‐Surface Synthesis of Peripherally Oxygen‐Annulated Porphyrins through C−O Bond Formation
inferred← citeshttps://doi.org/10.1002/aoc.1308openalex-snapshot
Spectroscopic studies of charge transfer complexes of meso‐tetra‐p‐tolylporphyrin and its zinc complex with some aromatic nitro acceptors in different organic solvents
inferred← citeshttps://doi.org/10.1002/aoc.2971openalex-snapshot
Synthesis, characterization and cytotoxic activity of 5,10,15,20‐tetrakis[4‐(triorganostannyloxy)phenyl]porphyrins
inferred← citeshttps://doi.org/10.1002/aoc.5055openalex-snapshot
Metalloporphyrins‐Al3+porous coordination polymers: Preparations, Characterizations and Catalytic Properties
inferred← citeshttps://doi.org/10.1002/aoc.649openalex-snapshot
The role of cobalt, copper, nickel, and zinc in the DNA replication inhibitory activity of p‐aminophenyl triphenylporphyrin
inferred← citeshttps://doi.org/10.1002/app.35022openalex-snapshot
Application of tin(IV) porphyrin complexes as novel catalysts for the synthesis of new copolyurethanes with cyclopeptide moiety
inferred← citeshttps://doi.org/10.1002/asia.201100533openalex-snapshot
Light‐Induced Electron Transfer over Distances of 5, 10, and 15 Å within Water‐Filled Yoctowells
inferred← citeshttps://doi.org/10.1002/asia.201201089openalex-snapshot
Facile Synthesis and Photophysical Properties of Sphere–Square Shape Amphiphiles Based on Porphyrin–[60]Fullerene Conjugates
inferred← citeshttps://doi.org/10.1002/asia.201601270openalex-snapshot
“To Twist or Not to Twist”: Figure‐of‐Eight and Planar Structures of Octaphyrins
inferred← citeshttps://doi.org/10.1002/asia.202100053openalex-snapshot
A New Potent Antimicrobial Metalloporphyrin
inferred← citeshttps://doi.org/10.1002/bio.4649openalex-snapshot
A signal‐switchable fluorescent probe for detection of HPO42− based on 5,10,15,20‐(4‐sulphonatophenyl)porphyrin (TPPS4)
inferred← citeshttps://doi.org/10.1002/bkcs.11042openalex-snapshot
Self‐assembling Helical Rod–Coil Peptoid Amphiphiles
inferred← citeshttps://doi.org/10.1002/cbic.202200095openalex-snapshot
Tetraphenylporphyrin Enters the Ring: First Example of a Complex between Highly Bulky Porphyrins and a Protein**
inferred← citeshttps://doi.org/10.1002/cctc.202201512openalex-snapshot
Hydrodechlorination of Alachlor Using a Molecular Electrocatalyst
inferred← citeshttps://doi.org/10.1002/chem.19950010111openalex-snapshot
5,10,15,20‐Tetraphenylsapphyrin‐Identification of a Pentapyrrolic Expanded Porphyrin in the Rothemund Synthesis
inferred← citeshttps://doi.org/10.1002/chem.19960021004openalex-snapshot
Porphyrin Synthesis by the “3+1” Approach: New Applications for an Old Methodology
inferred← citeshttps://doi.org/10.1002/chem.19970031122openalex-snapshot
2,3,7,8,12,13,17,18‐Octafluoro‐5,10,15,20‐Tetraphenylporphyrin: First Synthesis and X‐Ray Crystal Structure of the ZnII Complex
inferred← citeshttps://doi.org/10.1002/chem.200304995openalex-snapshot
Modulating Charge‐Transfer Interactions in Topologically Different Porphyrin–C60 Dyads
inferred← citeshttps://doi.org/10.1002/chem.200305045openalex-snapshot
Electronically Tuned Chiral Ruthenium Porphyrins: Extremely Stable and Selective Catalysts for Asymmetric Epoxidation and Cyclopropanation
inferred← citeshttps://doi.org/10.1002/chem.200401306openalex-snapshot
Giant meso–meso‐Linked Porphyrin Arrays of Micrometer Molecular Length and Their Fabrication
inferred← citeshttps://doi.org/10.1002/chem.200601691openalex-snapshot
Syntheses and Energy Transfer in Multiporphyrinic Arrays Self‐Assembled with Hydrogen‐Bonding Recognition Groups and Comparison with Covalent Steroidal Models
inferred← citeshttps://doi.org/10.1002/chem.200700054openalex-snapshot
Porphyrin, Phthalocyanine and Porphyrazine Derivatives with Multifluorenyl Substituents as Efficient Deep‐Red Emitters
inferred← citeshttps://doi.org/10.1002/chem.200701720openalex-snapshot
Light‐Harvesting Supramolecular Porphyrin Macrocycle Accommodating a Fullerene–Tripodal Ligand
inferred← citeshttps://doi.org/10.1002/chem.200800776openalex-snapshot
Two‐Dimensionally Extended Porphyrin Tapes: Synthesis and Shape‐Dependent Two‐Photon Absorption Properties
inferred← citeshttps://doi.org/10.1002/chem.200802166openalex-snapshot
Enhanced Electron‐Transfer Properties of Cofacial Porphyrin Dimers through π–π Interactions
inferred← citeshttps://doi.org/10.1002/chem.200900195openalex-snapshot
Coherently Aligned Porphyrin‐Appended Polynorbornenes
inferred← citeshttps://doi.org/10.1002/chem.200901362openalex-snapshot
Hydrogen‐Atom Abstraction Reactions by Manganese(V)– and Manganese(IV)–Oxo Porphyrin Complexes in Aqueous Solution
inferred← citeshttps://doi.org/10.1002/chem.200902161openalex-snapshot
Dendritic Porphyrin–Fullerene Conjugates: Efficient Light‐Harvesting and Charge‐Transfer Events
inferred← citeshttps://doi.org/10.1002/chem.201000760openalex-snapshot
Dendronizing and Metalating trans‐2 C60 Tetraaryl Porphyrins—A Versatile Approach Toward Water‐Soluble Donor–Acceptor Conjugates
inferred← citeshttps://doi.org/10.1002/chem.201002596openalex-snapshot
meso‐Aryl Phenanthroporphyrins: Synthesis and Spectroscopic Properties
inferred← citeshttps://doi.org/10.1002/chem.201100270openalex-snapshot
Microenvironment Engineering in ortho‐ and para‐Dendronized Metalloporphyrin–Fullerene Conjugates Involving a trans‐2‐Bisaddition Pattern
inferred← citeshttps://doi.org/10.1002/chem.201101432openalex-snapshot
Biomimetic Oxidation Reactions of a Naked Manganese(V)–Oxo Porphyrin Complex
inferred← citeshttps://doi.org/10.1002/chem.201300532openalex-snapshot
Nanoscopic Imaging of meso‐Tetraalkylporphyrins Prepared in High Yields Enabled by Montmorrilonite K10 and 3 Å Molecular Sieves
inferred← citeshttps://doi.org/10.1002/chem.201303676openalex-snapshot
Hückel and Möbius Expanded para‐Benziporphyrins: Synthesis and Aromaticity Switching
inferred← citeshttps://doi.org/10.1002/chem.201403677openalex-snapshot
An Efficient Synthesis of Porphyrins with Different meso Substituents that Avoids Scrambling in Aqueous Media
inferred← citeshttps://doi.org/10.1002/chem.201405039openalex-snapshot
Layer‐by‐Layer Assemblies of Catechol‐Functionalized TiO2 Nanoparticles and Porphyrins through Electrostatic Interactions
inferred← citeshttps://doi.org/10.1002/chem.201501254openalex-snapshot
Synthesis and Atropisomerism of Cascaded Tetraphenylporphyrin–[60]Fullerene Hybrids
inferred← citeshttps://doi.org/10.1002/chem.201601857openalex-snapshot
Nucleophilic Aromatic Substitution on Pentafluorophenyl‐Substituted Dipyrranes and Tetrapyrroles as a Route to Multifunctionalized Chromophores for Potential Application in Photodynamic Therapy
inferred← citeshttps://doi.org/10.1002/chem.201603789openalex-snapshot
Three Short Stories about Hexaarylbenzene–Porphyrin Scaffolds
inferred← citeshttps://doi.org/10.1002/chem.201605872openalex-snapshot
Directing the Self‐Assembly Behaviour of Porphyrin‐Based Supramolecular Systems
inferred← citeshttps://doi.org/10.1002/chem.201701619openalex-snapshot
Mechanochemical Synthesis of Phosphazane‐Based Frameworks
inferred← citeshttps://doi.org/10.1002/chem.201704222openalex-snapshot
Fluorescence Commutation and Surface Photopatterning with Porphyrin Tetradithienylethene Switches
inferred← citeshttps://doi.org/10.1002/chem.201803684openalex-snapshot
Superbenzene–Porphyrin Gas‐Phase Architectures Derived from Intermolecular Dispersion Interactions
inferred← citeshttps://doi.org/10.1002/chem.201904718openalex-snapshot
A Comprehensive Study on Tetraaryltetrabenzoporphyrins
inferred← citeshttps://doi.org/10.1002/chem.201905602openalex-snapshot
Control over the Redox Cooperative Mechanism of Radical Carbene Transfer Reactions for the Efficient Active‐Metal‐Template Synthesis of [2]Rotaxanes
inferred← citeshttps://doi.org/10.1002/chem.201905637openalex-snapshot
Atropisomers of meso Tetra(N‐Mesyl Pyrrol‐2‐yl) Porphyrins: Synthesis, Isolation and Characterization of All‐Pyrrolic Porphyrins
inferred← citeshttps://doi.org/10.1002/chem.202002813openalex-snapshot
Enhanced Electrocatalytic Activity of a Zinc Porphyrin for CO2 Reduction: Cooperative Effects of Triazole Units in the Second Coordination Sphere
inferred← citeshttps://doi.org/10.1002/chem.202003885openalex-snapshot
Modular Synthesis of trans‐A2B2‐Porphyrins with Terminal Esters: Systematically Extending the Scope of Linear Linkers for Porphyrin‐Based MOFs
inferred← citeshttps://doi.org/10.1002/chem.202200056openalex-snapshot
Strain‐Induced Ring Expansion Reactions of Calix[3]pyrrole‐Related Macrocycles
inferred← citeshttps://doi.org/10.1002/chem.202300940openalex-snapshot
Strong and Tunable Near‐Infrared Circular Dichroism in Helical Tetrapyrrole Complexes
inferred← citeshttps://doi.org/10.1002/chin.198741321openalex-snapshot
ChemInform Abstract: Rothemund and Adler‐Longo Reactions Revisited: Synthesis of Tetraphenylporphyrins Under Equilibrium Conditions.
inferred← citeshttps://doi.org/10.1002/chin.201211224openalex-snapshot
ChemInform Abstract: Large Molecules Containing Icosahedral Boron Clusters Designed for Potential Applications
inferred← citeshttps://doi.org/10.1002/chir.10253openalex-snapshot
Molecular engineering of extended chiral and enantiopure multiporphyrinic architectures: Towards the control of their physico-chemical properties
inferred← citeshttps://doi.org/10.1002/cjoc.19900080513openalex-snapshot
The synthesis of fluorine‐containing porphyrins
inferred← citeshttps://doi.org/10.1002/cjoc.19920100212openalex-snapshot
The synthesis of perfluoroalkyl‐substituted tetrakisphenylporphyrins
inferred← citeshttps://doi.org/10.1002/cjoc.19950130510openalex-snapshot
Substituent effects on chloro meso‐tetra‐ortho‐alkylphenylporphinato iron catalyzed biomimetic oxidation of cyclohexane
inferred← citeshttps://doi.org/10.1002/cjoc.200590431openalex-snapshot
Synthesis of 5,10,15,20‐Tetra[4‐(N‐ethylpiperazinyl)phenyl]‐porphyrin and Its Interaction with DNA
inferred← citeshttps://doi.org/10.1002/cjoc.201090063openalex-snapshot
Fast and Eco‐friendly Synthesis of Dipyrromethanes by H2SO4·SiO2 Catalysis under Solvent‐free Conditions
inferred← citeshttps://doi.org/10.1002/cjoc.201200321openalex-snapshot
Synthesis and Characterization of 5,10‐ and 5,15‐Disubstituted Porphodimethenes
inferred← citeshttps://doi.org/10.1002/cjoc.201900177openalex-snapshot
Order from Chaos: Self‐Assembly of Nanoprism from a Mixture of Tetratopic Terpyridine‐Porphyrin Conformers
inferred← citeshttps://doi.org/10.1002/cjoc.202200257openalex-snapshot
Novel Porphyrin‐Containing Polymer Based Memristor for Synaptic Plasticity Simulation
inferred← citeshttps://doi.org/10.1002/cmtd.202000055openalex-snapshot
Addressing Environmental Challenges of Porphyrin Mixtures Obtained from Statistical Syntheses
inferred← citeshttps://doi.org/10.1002/cphc.202500150openalex-snapshot
Porphyrin–Peptide Conjugates: Functional Self‐Assembled Nanomaterials for Biomedical and Energy Conversion Applications
inferred← citeshttps://doi.org/10.1002/cplu.202200228openalex-snapshot
Synthesis of Photosensitizers Based on Tetrapyrrolic Macrocycles for Combination with Antibiotics: Dual Inactivation of Bacteria
inferred← citeshttps://doi.org/10.1002/cptc.202500086openalex-snapshot
Star‐Shaped Fluorescent Porphyrins with Impressive Two‐Photon‐Absorption Cross‐Sections for Oxygen Sensitization: The Impact of Periphery‐Conjugated Electron‐Releasing Groups
inferred← citeshttps://doi.org/10.1002/cssc.201402464openalex-snapshot
Ecofriendly Porphyrin Synthesis by using Water under Microwave Irradiation
inferred← citeshttps://doi.org/10.1002/cssc.201802198openalex-snapshot
Three Generations of Cobalt Porphyrins as Catalysts in the Oxidation of Cycloalkanes
inferred← citeshttps://doi.org/10.1002/cssc.202002718openalex-snapshot
Through‐Space Electrostatic Interactions Surpass Classical Through‐Bond Electronic Effects in Enhancing CO2 Reduction Performance of Iron Porphyrins
inferred← citeshttps://doi.org/10.1002/ejic.200300918openalex-snapshot
Conformational Effects on the Photoinduced Energy Transfer in a Star‐Shaped Pentaporphyrin with Nucleosidic Linkers
inferred← citeshttps://doi.org/10.1002/ejic.200700845openalex-snapshot
The N‐Acylated Derivatives of Parent Complex [{(μ‐SCH2)2NH}Fe2(CO)6] as Active Site Models of Fe‐Only Hydrogenases: Synthesis, Characterization, and Related Properties
inferred← citeshttps://doi.org/10.1002/ejic.200800253openalex-snapshot
Solvent Effects on Catalytic Epoxidation of Alkenes by Tetra‐n‐butylammonium Periodate and (Tetraarylporphyrinato)manganese(III)
inferred← citeshttps://doi.org/10.1002/ejic.201100025openalex-snapshot
Synthesis, Structure, and Photophysical Properties of Some Gadolinium(III) Porphyrinate Complexes
inferred← citeshttps://doi.org/10.1002/ejic.201100763openalex-snapshot
Insights into the Mechanism of the Ruthenium–Porphyrin‐Catalysed Allylic Amination of Olefins by Aryl Azides
inferred← citeshttps://doi.org/10.1002/ejic.201200868openalex-snapshot
High‐Yielding Synthesis of β‐Octaalkyl‐meso‐(bromophenyl)‐Substituted Porphyrins and X‐ray Study of Axial Complexes of Their Zinc Complexes with THF and 1,4‐Dioxane
inferred← citeshttps://doi.org/10.1002/ejic.201201437openalex-snapshot
Nanoaggregates of Simple Mn Porphyrin Complexes as Catalysts for the Selective Oxidation of Hydrocarbons
inferred← citeshttps://doi.org/10.1002/ejic.201300038openalex-snapshot
Synthesis, Structures, and Properties of Diiron Azadithiolate Complexes Containing a Subphthalocyanine Moiety as Biomimetic Models for [FeFe]‐Hydrogenases
inferred← citeshttps://doi.org/10.1002/ejic.201402008openalex-snapshot
Intermolecular Interactions in Fluorinated Tetraarylporphyrins: An Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1002/ejic.201402800openalex-snapshot
Mono‐Oxido‐Bridged Heterobimetallic and Heterotrimetallic Compounds Containing Titanium(IV) and Chromium(III)
showing the first 200 of 1446 · page through all 1446
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.