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meso‐Aryl [20]π Homoporphyrin: The Simplest Expanded Porphyrin with the Smallest Möbius Topology

https://doi.org/10.1002/anie.201709859
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inferredcites →https://doi.org/10.1002/ange.19750871510openalex-snapshot
Einschiebung einer Äthoxycarbonylmethylen‐Gruppierung in eine NiN‐Bindung von meso‐Tetraphenylporphinatonickel(II)
inferredcites →https://doi.org/10.1002/ange.19951070309openalex-snapshot
Aromatizität und Antiaromatizität in fünfgliedrigen C4H4X‐Ringsystemen: beschreibbar durch „klassische” und „magnetische” Konzepte
inferredcites →https://doi.org/10.1002/ange.200200561openalex-snapshot
Synthesechemie expandierter Porphyrine
inferredcites →https://doi.org/10.1002/ange.200603249openalex-snapshot
“Metamorphose” von Tetrapyrrolmakrocyclen
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.200705568openalex-snapshot
Der Porphyrin‐Twist: Hückel‐ und Möbius‐Aromatizität
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.200902677openalex-snapshot
Thermal Fusion Reactions of meso‐(3‐Thienyl) Groups in [26]Hexaphyrins to Produce Möbius Aromatic Molecules
inferredcites →https://doi.org/10.1002/ange.200906017openalex-snapshot
A Stable Organic Radical Delocalized on a Highly Twisted π System Formed Upon Palladium Metalation of a Möbius Aromatic Hexaphyrin
inferredcites →https://doi.org/10.1002/ange.201001765openalex-snapshot
Möbius Antiaromatic Bisphosphorus Complexes of [30]Hexaphyrins
inferredcites →https://doi.org/10.1002/ange.201002282openalex-snapshot
Metal Complexes of Chiral Möbius Aromatic [28]Hexaphyrin(1.1.1.1.1.1): Enantiomeric Separation, Absolute Stereochemistry, and Asymmetric Synthesis
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.201003909openalex-snapshot
Expandierte Porphyrine: überraschende Strukturen, elektronische Eigenschaften und Reaktivitäten
inferredcites →https://doi.org/10.1002/ange.201005334openalex-snapshot
Redox‐Induced Palladium Migrations that Allow Reversible Topological Changes between Palladium(II) Complexes of Möbius Aromatic [28]Hexaphyrin and Hückel Aromatic [26]Hexaphyrin
inferredcites →https://doi.org/10.1002/ange.201208147openalex-snapshot
A Möbius Antiaromatic Complex as a Kinetically Controlled Product in Phosphorus Insertion to a [32]Heptaphyrin
inferredcites →https://doi.org/10.1002/ange.201408506openalex-snapshot
PdII Complexes of [44]‐ and [46]Decaphyrins: The Largest Hückel Aromatic and Antiaromatic, and Möbius Aromatic Macrocycles
inferredcites →https://doi.org/10.1002/ange.201500099openalex-snapshot
A Möbius Aromatic [28]Hexaphyrin Bearing a Diethylamine Group: A Rigid but Smooth Conjugation Circuit
inferredcites →https://doi.org/10.1002/anie.197505671openalex-snapshot
Insertion of an Ethoxycarbonylmethylene Moiety into a NiN Bond of meso‐Tetraphenylporphinatonickel(II)
inferredcites →https://doi.org/10.1002/anie.199503371openalex-snapshot
Aromaticity and Antiaromaticity in Five‐Membered C4H4X Ring Systems: “Classical” and “Magnetic” Concepts May Not Be “Orthogonal”
inferredcites →https://doi.org/10.1002/anie.200200561openalex-snapshot
Synthetic Expanded Porphyrin Chemistry
inferredcites →https://doi.org/10.1002/anie.200603249openalex-snapshot
Metamorphosis of Tetrapyrrole Macrocycles
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.200705568openalex-snapshot
The Porphyrin Twist: Hückel 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.200902677openalex-snapshot
Thermal Fusion Reactions of meso‐(3‐Thienyl) Groups in [26]Hexaphyrins to Produce Möbius Aromatic Molecules
inferredcites →https://doi.org/10.1002/anie.200906017openalex-snapshot
A Stable Organic Radical Delocalized on a Highly Twisted π System Formed Upon Palladium Metalation of a Möbius Aromatic Hexaphyrin
inferredcites →https://doi.org/10.1002/anie.201001765openalex-snapshot
Möbius Antiaromatic Bisphosphorus Complexes of [30]Hexaphyrins
inferredcites →https://doi.org/10.1002/anie.201002282openalex-snapshot
Metal Complexes of Chiral Möbius Aromatic [28]Hexaphyrin(1.1.1.1.1.1): Enantiomeric Separation, Absolute Stereochemistry, and Asymmetric Synthesis
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.201003909openalex-snapshot
Expanded Porphyrins: Intriguing Structures, Electronic Properties, and Reactivities
inferredcites →https://doi.org/10.1002/anie.201005334openalex-snapshot
Redox‐Induced Palladium Migrations that Allow Reversible Topological Changes between Palladium(II) Complexes of Möbius Aromatic [28]Hexaphyrin and Hückel Aromatic [26]Hexaphyrin
inferredcites →https://doi.org/10.1002/anie.201208147openalex-snapshot
A Möbius Antiaromatic Complex as a Kinetically Controlled Product in Phosphorus Insertion to a [32]Heptaphyrin
inferredcites →https://doi.org/10.1002/anie.201408506openalex-snapshot
PdII Complexes of [44]‐ and [46]Decaphyrins: The Largest Hückel Aromatic and Antiaromatic, and Möbius Aromatic Macrocycles
inferredcites →https://doi.org/10.1002/anie.201500099openalex-snapshot
A Möbius Aromatic [28]Hexaphyrin Bearing a Diethylamine Group: A Rigid but Smooth Conjugation Circuit
inferredcites →https://doi.org/10.1002/asia.201500170openalex-snapshot
Aromaticity Switching in Porphyrinoids
inferredcites →https://doi.org/10.1002/asia.201600025openalex-snapshot
Möbius Aromatic Core‐Modified Heterocyclic [20] Macrocycles (4.1.1) with a Protruding N‐Methyl Pyrrole Ring
inferredcites →https://doi.org/10.1002/chem.201100757openalex-snapshot
Möbius Aromatic [28]Hexaphyrin Phosphonium Adducts
inferredcites →https://doi.org/10.1002/chem.201200511openalex-snapshot
Viability of Möbius Topologies in [26]‐ and [28]Hexaphyrins
inferredcites →https://doi.org/10.1002/chem.201200762openalex-snapshot
Regioselective Palladation of a Möbius Aromatic [28]Hexaphyrin(1.1.1.1.1.1) PdII Complex
inferredcites →https://doi.org/10.1002/chem.201402929openalex-snapshot
SiIV Incorporation into a [28]Hexaphyrin That Triggered Formation of Möbius Aromatic Molecules
inferredcites →https://doi.org/10.1002/chem.201505116openalex-snapshot
[32]π Fused Core‐Modified Heptaphyrin with Möbius Aromaticity
inferredcites →https://doi.org/10.1002/ejoc.201501182openalex-snapshot
Synthesis, Structure, Spectral and Electrochemical Properties of [20]Dioxahomoporphyrins and Covalently Linked Dioxahomoporphyrin–Porphyrin Dyads
inferredcites →https://doi.org/10.1016/s0040-4039(00)75031-3openalex-snapshot
New tetrapyrrolic macrocycles. 18 and 20π electrons homoporphyrins and related compounds
inferredcites →https://doi.org/10.1016/s0040-4039(01)89474-0openalex-snapshot
Hűckel molecular orbitals of Mőbius-type conformations of annulenes
inferredcites →https://doi.org/10.1016/s0040-4039(01)91848-9openalex-snapshot
Homoporphyrins I preparation - structure
inferredcites →https://doi.org/10.1016/s0040-4039(01)91849-0openalex-snapshot
Homoporphyrins II thermal rearrangements
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00021openalex-snapshot
Development of Ion Chemosensors Based on Porphyrin Analogues
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00313openalex-snapshot
Control and Switching of Aromaticity in Various All-Aza-Expanded Porphyrins: Spectroscopic and Theoretical Analyses
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00345openalex-snapshot
Porphycenes and Related Isomers: Synthetic Aspects
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00371openalex-snapshot
Chemistry of meso -Aryl-Substituted Expanded Porphyrins: Aromaticity and Molecular Twist
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00411openalex-snapshot
Annulated Isomeric, Expanded, and Contracted Porphyrins
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00434openalex-snapshot
Synthesis of Corroles and Their Heteroanalogs
inferredcites →https://doi.org/10.1021/acs.chemrev.6b00507openalex-snapshot
Smaragdyrins and Sapphyrins Analogues
inferredcites →https://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
inferredcites →https://doi.org/10.1021/ar980117gopenalex-snapshot
Sapphyrins: Versatile Anion Binding Agents
inferredcites →https://doi.org/10.1021/ci00011a011openalex-snapshot
Crystallographic studies of inter- and intramolecular interactions reflected in aromatic character of .pi.-electron systems
inferredcites →https://doi.org/10.1021/cr400088wopenalex-snapshot
Subphthalocyanines, Subporphyrazines, and Subporphyrins: Singular Nonplanar Aromatic Systems
inferredcites →https://doi.org/10.1021/cr950078bopenalex-snapshot
Expanded Porphyrins and Their Heterologs
inferredcites →https://doi.org/10.1021/cr990326uopenalex-snapshot
Structural Aspects of Aromaticity
inferredcites →https://doi.org/10.1021/ic50158a005openalex-snapshot
Highly distorted homoporphyrin complex. Crystal and molecular structure of the (10H-10-hydroxyl-21-ethoxycarbonyl-5,10,15,20-tetraphenyl-21-homoporphinato nickel (II)
inferredcites →https://doi.org/10.1021/ja00047a061openalex-snapshot
Rosarin: a new, easily prepared hexapyrrolic expanded porphyrin
inferredcites →https://doi.org/10.1021/ja00359a012openalex-snapshot
Sapphyrins: novel aromatic pentapyrrolic macrocycles
inferredcites →https://doi.org/10.1021/ja005588oopenalex-snapshot
Bis(azafulvene) as a Versatile Building Block for Giant Cyclopolypyrroles: X-ray Crystal Structure of [64]Hexadecaphyrin(1.0.1.0.1.0.1.0.1.0.1.0.1.0.1.0)
inferredcites →https://doi.org/10.1021/ja00839a024openalex-snapshot
New homoporphyrin system. 21-Ethoxycarbonyl-5,10,15,20-tetraphenyl-21H-21-homoporphine. Crystal structure and molecular stereochemistry of the nickel(II) complex
inferredcites →https://doi.org/10.1021/ja00854a038openalex-snapshot
Rearrangement of N-substituted porphyrins. Preparation and structure of homoporphyrins
inferredcites →https://doi.org/10.1021/ja00854a039openalex-snapshot
Acid catalyzed isomerization and thermal rearrangement of nickel homoporphyrins
inferredcites →https://doi.org/10.1021/ja7100483openalex-snapshot
Möbius Aromaticity in N-Fused [24]Pentaphyrin upon Rh(I) Metalation
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/ja902836xopenalex-snapshot
Facile Formation of a Benzopyrane-Fused [28]Hexaphyrin That Exhibits Distinct Möbius Aromaticity
inferredcites →https://doi.org/10.1021/ja909744zopenalex-snapshot
Protonated [4n]π and [4n+2]π Octaphyrins Choose Their Möbius/Hückel Aromatic Topology
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/jo00429a019openalex-snapshot
New tetrapyrrolic macrocycles. 18 and 20 .pi. Electron homoporphyrins
inferredcites →https://doi.org/10.1021/jo501724dopenalex-snapshot
Stable Nonaromatic [20]Dithiaporphyrin (2.1.1.1) Macrocycles: Synthesis, Structure, Spectral, Electrochemical, and Metal Ion Sensing Studies
inferredcites →https://doi.org/10.1021/jp0034426openalex-snapshot
Delocalization of Electrons in Molecules
inferredcites →https://doi.org/10.1021/jp207731kopenalex-snapshot
Solvent- and Temperature-Dependent Conformational Changes between Hückel Antiaromatic and Möbius Aromatic Species in meso-Trifluoromethyl Substituted [28]Hexaphyrins
inferredcites →https://doi.org/10.1021/jp8111205openalex-snapshot
Temperature-Dependent Conformational Change of meso-Hexakis(pentafluorophenyl) [28]Hexaphyrins(1.1.1.1.1.1) into Möbius Structures
inferredcites →https://doi.org/10.1021/ol200668aopenalex-snapshot
meso-Aryl Triphyrin(2.1.1)
inferredcites →https://doi.org/10.1021/ol802351ropenalex-snapshot
9,10,19,20-Tetraarylporphycenes
inferredcites →https://doi.org/10.1038/nature02224openalex-snapshot
Synthesis of a Möbius aromatic hydrocarbon
inferredcites →https://doi.org/10.1038/nchem.172openalex-snapshot
Möbius aromaticity and antiaromaticity in expanded porphyrins
inferredcites →https://doi.org/10.1039/b104004aopenalex-snapshot
The first bis-Rh(i) metal complex of N-confused porphyrin
inferredcites →https://doi.org/10.1039/b807066kopenalex-snapshot
Ring expansions and contractions of metalloporphyrins
inferredcites →https://doi.org/10.1039/b905859aopenalex-snapshot
Bis-rhodium hexaphyrins: metalation of [28]hexaphyrin and a smooth Hückel aromatic–antiaromatic interconversion
inferredcites →https://doi.org/10.1039/b925417jopenalex-snapshot
Aromaticity and photophysical properties of various topology-controlled expanded porphyrins
inferredcites →https://doi.org/10.1039/c1cc10534eopenalex-snapshot
Expanded porphyrins and aromaticity
inferredcites →https://doi.org/10.1039/c1cc14633eopenalex-snapshot
Blooming of confused porphyrinoids—fusion, expansion, contraction, and more confusion
inferredcites →https://doi.org/10.1039/c2cs35418gopenalex-snapshot
π-Extended isomeric and expanded porphyrins
inferredcites →https://doi.org/10.1039/c39740000884openalex-snapshot
A novel homoporphyrin system: crystal structure of the nickel complex
inferredcites →https://doi.org/10.1039/c3cc47908kopenalex-snapshot
Deprotonation induced formation of Möbius aromatic [32]heptaphyrins
inferredcites →https://doi.org/10.1039/c4cp05745gopenalex-snapshot
Möbius–Hückel topology switching in an expanded porphyrin cation radical as studied by EPR and ENDOR spectroscopy
inferredcites →https://doi.org/10.1039/j39710003664openalex-snapshot
Ring expansion of prophins with ethoxycarbonylnitrene

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.4654383openalex-extracted
Theoretical Exploration on the Aromaticity Regulation of Prophyrazine by (De)Protonation and (De)Hydrogenation
inferred← citeshttps://doi.org/10.1002/ange.202112023openalex-snapshot
Tetrabromo[36]octaphyrin: A Promising Precursor of Directly Fused Porphyrin(2.1.1.1) Dimer and meso‐α Fused N‐Confused Porphyrin Dimer
inferred← citeshttps://doi.org/10.1002/ange.202302662openalex-snapshot
Rearrangements of Internally‐bridged Octaphyrin(1.1.1.1.1.1.1.1)s to Porphyrin Dimers
inferred← citeshttps://doi.org/10.1002/anie.202112023openalex-snapshot
Tetrabromo[36]octaphyrin: A Promising Precursor of Directly Fused Porphyrin(2.1.1.1) Dimer and meso‐α Fused N‐Confused Porphyrin Dimer
inferred← citeshttps://doi.org/10.1002/anie.202302662openalex-snapshot
Rearrangements of Internally‐bridged Octaphyrin(1.1.1.1.1.1.1.1)s to Porphyrin Dimers
inferred← citeshttps://doi.org/10.1002/anie.4566077openalex-snapshot
Triply N‐Confused Hexaphyrins(1.1.1.1.1.0) Synthesized From N‐Confused Hexaphyrin(2.1.1.1.1.1): Aromaticity Modulation, Metal Coordination, and Photothermal Conversion
inferred← citeshttps://doi.org/10.1002/asia.202401548openalex-snapshot
Twists and Loops: Exploring Lemniscular Vinylogous Benzioctaphyrin(2.0.1.0.2.0.1.0)
inferred← citeshttps://doi.org/10.1002/asia.202500856openalex-snapshot
Siamese Twin Homocarbaporphyrin Dimer: Nonplanar Architecture, Localized Conjugation and Bis‐B III Complex
inferred← citeshttps://doi.org/10.1002/chem.201803552openalex-snapshot
24π Core‐Modified Nonfused Pentaphyrin with Möbius Aromaticity
inferred← citeshttps://doi.org/10.1002/chem.201900495openalex-snapshot
Homocarbaporphyrinoids: The m‐o‐m and p‐o‐p Terphenyl Embedded Expanded Porphyrin Analogues and Their RhI Complexes
inferred← citeshttps://doi.org/10.1002/ejoc.201800900openalex-snapshot
Covalently Linked meso‐BODIPYnyl Dithiahomoporphyrins: Synthesis and Properties
inferred← citeshttps://doi.org/10.1002/ejoc.202001165openalex-snapshot
Synthesis and Structure of meso‐Substituted Dibenzihomoporphyrins
inferred← citeshttps://doi.org/10.1002/tcr.202200144openalex-snapshot
Synthesis and Properties of Stable 20π Porphyrinoids
inferred← citeshttps://doi.org/10.1007/s41061-025-00506-yopenalex-snapshot
Dipyrroethanes/Dipyrroethenes: New Precursors for Porphyrinoids
inferred← citeshttps://doi.org/10.1016/b978-0-08-102788-2.00017-9openalex-snapshot
Eight-Membered and Larger Rings
inferred← citeshttps://doi.org/10.1016/b978-0-12-814805-1.00009-0openalex-snapshot
Synthesis of theoretically interesting molecules
inferred← citeshttps://doi.org/10.1016/j.comptc.2024.114501openalex-snapshot
Theoretical exploration on the aromaticity regulation of prophyrazine by (de)protonation and (de)hydrogenation
inferred← citeshttps://doi.org/10.1016/j.dyepig.2021.109612openalex-snapshot
Stable thiophene-embedded N-confused homoporphyrins: Partial conjugation, fusion and fluoride binding
inferred← citeshttps://doi.org/10.1016/j.tet.2021.132126openalex-snapshot
Synthesis of non-aromatic stable di-para-benzihomoporphyrins
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c03782openalex-snapshot
Meso -Modified Porphyrinoids: Stimuli-Driven Conformational Plasticity, Modulation of π-Conjugation, and Bis-Rh(I) Complexation
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b00977openalex-snapshot
[30]Hexaphyrin(2.1.2.1.2.1) as Aromatic Planar Ligand and Its Trinuclear Rhodium(I) Complex
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.9b02905openalex-snapshot
Core-Modified Pentaphyrins(2.1.1.1.1) and Bis(difluoroborane) Complex: Synthesis, Structure, and Spectral and Redox Properties
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00871openalex-snapshot
Di-(m-m-m)terphenyl-Embedded Decaphyrin and Its Bis-Rh(I) Complex
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04614openalex-snapshot
Structurally Isomerized Bis-Biphenyl Moieties Embedded in Hexaphyrin(3.1.1.3.1.1) and Octaphyrin(1.1.1.0.1.1.1.0)
inferred← citeshttps://doi.org/10.1021/acscentsci.8b00086openalex-snapshot
Coarctate and Möbius: The Helical Orbitals of Allene and Other Cumulenes
inferred← citeshttps://doi.org/10.1021/acsomega.1c05444openalex-snapshot
Recent Advances in the Design and Syntheses of Porphyrinoids by Embedding Higher Analogues of Arene and Pyridine Units
inferred← citeshttps://doi.org/10.1039/d1qo01946eopenalex-snapshot
Synthesis of N-fused dithia and dibenzi homoporphyrins
inferred← citeshttps://doi.org/10.1039/d3nj03432aopenalex-snapshot
Unveiling protonated form of 2,6-di- m -phenylpyridine embedded isosmaragdyrin analogue and its organo-Pd( ii ) complex
inferred← citeshttps://doi.org/10.1073/pnas.2102310118openalex-snapshot
Electrophilic aromatic substitution reactions of compounds with Craig-Möbius aromaticity
inferred← citeshttps://doi.org/10.1142/s1088424621501108openalex-snapshot
Synthesis and properties of covalently linked di-p-benzihomoporphyrin-BODIPY conjugates
inferred← citeshttps://doi.org/10.1142/s1088424622500900openalex-snapshot
Serendipitous formation of meso-free corroles in the [3+1] porphyrin and [3+2] sapphyrin syntheses
inferred← citeshttps://doi.org/10.1515/pac-2025-0482openalex-snapshot
Topological innovation in molecular design: advances in Möbius architectures for functional materials
inferred← citeshttps://doi.org/10.5772/intechopen.86206openalex-snapshot
Technological Applications of Porphyrins and Related Compounds: Spintronics and Micro-/Nanomotors
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