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Aromaticity and Antiaromaticity in the Low-Lying Electronic States of Cyclooctatetraene
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1521-3773(19980803)37:13/14<1945::aid-anie1945>3.0.co;2-eopenalex-snapshot
Consequences of Triplet Aromaticity in 4nπ-Electron Annulenes: Calculation of Magnetic Shieldings for Open-Shell Species
inferredcites →https://doi.org/10.1002/1521-3773(20010119)40:2<362::aid-anie362>3.0.co;2-zopenalex-snapshot
Counter-Rotating Ring Currents in Coronene and Corannulene
inferredcites →https://doi.org/10.1016/0301-0104(95)00052-popenalex-snapshot
Accurate magnetizabilities of the isoelectronic series BeH−, BH, and CH+. The MCSCF-GIAO approach
inferredcites →https://doi.org/10.1016/j.cplett.2007.11.053openalex-snapshot
Ring-current aromaticity in open-shell systems
inferredcites →https://doi.org/10.1016/s0009-2614(03)00349-xopenalex-snapshot
Ring-current aromaticity in triplet states of 4n π electron monocycles
inferredcites →https://doi.org/10.1021/ed048p92openalex-snapshot
The symmetries and multiplicities of electronic states in polyatomic molecules
inferredcites →https://doi.org/10.1021/j100025a020openalex-snapshot
The Electronic Structure of Cyclooctatetraene and the Modern Valence-Bond Understanding of Antiaromaticity
inferredcites →https://doi.org/10.1021/ja00040a071openalex-snapshot
CASSCF calculations find that a D8h geometry is the transition state for double bond shifting in cyclooctatetraene
inferredcites →https://doi.org/10.1021/ja00091a039openalex-snapshot
IGLO Study of Benzene and Some of Its Isomers and Related Molecules. Search for Evidence of the Ring Current Model
inferredcites →https://doi.org/10.1021/ja00769a025openalex-snapshot
Quantum organic photochemistry. II. Resonance and aromaticity in the lowest 3.pi..pi.* state of cyclic hydrocarbons
inferredcites →https://doi.org/10.1021/ja00805a006openalex-snapshot
Localized magnetic susceptibility anisotropies
inferredcites →https://doi.org/10.1021/ja020741vopenalex-snapshot
Cyclooctatetraene Computational Photo- and Thermal Chemistry: A Reactivity Model for Conjugated Hydrocarbons
inferredcites →https://doi.org/10.1021/ja960582dopenalex-snapshot
Nucleus-Independent Chemical Shifts: A Simple and Efficient Aromaticity Probe
inferredcites →https://doi.org/10.1021/ja9719135openalex-snapshot
An Evaluation of the Aromaticity of Inorganic Rings: Refined Evidence from Magnetic Properties
inferredcites →https://doi.org/10.1021/jp8037335openalex-snapshot
Ground- and Excited-State Aromaticity and Antiaromaticity in Benzene and Cyclobutadiene
inferredcites →https://doi.org/10.1021/ol016217vopenalex-snapshot
Dissected Nucleus-Independent Chemical Shift Analysis of π-Aromaticity and Antiaromaticity
inferredcites →https://doi.org/10.1021/ol0529546openalex-snapshot
Which NICS Aromaticity Index for Planar π Rings Is Best?
inferredcites →https://doi.org/10.1039/b706135hopenalex-snapshot
Theory and computation of nuclear magnetic resonance parameters
inferredcites →https://doi.org/10.1063/1.1535904openalex-snapshot
Calculations of nuclear magnetic shielding in paramagnetic molecules
inferredcites →https://doi.org/10.1063/1.462209openalex-snapshot
Second-order perturbation theory with a complete active space self-consistent field reference function
inferredcites →https://doi.org/10.1063/1.466812openalex-snapshot
Multiconfigurational self-consistent field calculations of nuclear shieldings using London atomic orbitals
inferredcites →https://doi.org/10.1063/1.470928openalex-snapshot
Calculation of nuclear magnetic resonance shieldings and magnetic susceptibilities using multiconfiguration Hartree–Fock wave functions and local gauge origins
inferredcites →https://doi.org/10.1063/1.475388openalex-snapshot
Potential energy surface of cyclooctatetraene
inferredcites →https://doi.org/10.1080/00268970050032792openalex-snapshot
Ring currents in six-membered heterocycles: the diazaborinines (CH)2B2N2
inferredcites →https://doi.org/10.1126/science.272.5267.1456openalex-snapshot
Transition-State Spectroscopy of Cyclooctatetraene
inferredcites →https://doi.org/10.5860/choice.32-2146openalex-snapshot
Group theory in chemistry and spectroscopy: a simple guide to advanced usage
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.12688/openreseurope.19690.1zenodo-depositor-declared
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inferred← citeshttps://doi.org/10.1002/9781119085928.ch2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/9781119643098.ch2openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201603631openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201611431openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.201706861openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202001934openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202100261openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202106490openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.202218156openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.6799620openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201603631openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201611431openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201706861openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202001934openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202100261openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202106490openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202218156openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.6799620openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/asia.201500897openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/asia.201801821openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201300008openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201303955openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201402577openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201504924openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201701404openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.201804292openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202001804openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202102351openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202103122openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202103896openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.202203748openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/chem.71596openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cphc.201501019openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cphc.202300038openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cphc.202400271openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cphc.202400758openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cphc.202500335openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cplu.201800307openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cplu.201900066openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cptc.201800268openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cptc.202300291openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.4455openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/poc.70012openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/slct.202103919openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/slct.202506584openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/wcms.1404openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/978-4-431-55357-1_4openalex-snapshot
Planar Cyclooctatetraenes and Related Ring Systems: Antiaromaticity and Applications
inferred← citeshttps://doi.org/10.1007/s00214-019-2459-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00214-023-02989-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00894-015-2683-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10593-014-1482-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11224-012-9991-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11224-016-0882-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s12039-023-02230-wopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-409547-2.14768-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-821978-2.00061-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-822723-7.00012-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-12-822723-7.00013-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/bs.arnmr.2022.07.001openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chemphys.2016.02.005openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.chempr.2018.03.020openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cjsc.2024.100273openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.comptc.2026.116031openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cplett.2015.06.018openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.cplett.2019.03.051openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2012.05.056openalex-snapshot
A theoretical NMR study of the structure of benzynes and some of their carbocyclic and heterocyclic analogs
inferred← citeshttps://doi.org/10.1016/j.tet.2013.06.072openalex-snapshot
A theoretical study on the aromaticity of benzene and related derivatives incorporating a C–C C–C fragment
inferred← citeshttps://doi.org/10.1016/j.tet.2014.12.058openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tet.2016.06.050openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.accounts.3c00605openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00313openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.5b01010openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.5c00578openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.6b02460openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.7b00906openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.9b01858openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.joc.9b03472openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.0c01655openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.0c08594openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.0c08926openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.2c07059openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.3c00485openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.6b11684openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.6c03133openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpca.6c03758openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpcc.4c05336openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.jpclett.1c01908openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03254openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr100228ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/cr300471vopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ct3000553openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ct4007508openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/ja908161ropenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.0c06327openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.1c09324openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.2c06448openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.2c10088openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.3c10207openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.4c18623openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.5b04047openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.7b08021openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jacs.9b13769openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo401853zopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo500098hopenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jo9025868openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jp3032397openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jp311536copenalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jp4108014openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jp411660eopenalex-snapshot
Investigation of the Electronic Structures of Organolanthanide Sandwich Complex Anions by Photoelectron Spectroscopy: 4f Orbital Contribution in the Metal–Ligand Interaction
inferred← citeshttps://doi.org/10.1021/jp503220qopenalex-snapshot
Photoisomerization of Silyl-Substituted Cyclobutadiene Induced by σ → π* Excitation: A Computational Study
inferred← citeshttps://doi.org/10.1021/jp904335jopenalex-snapshot
Aromaticity Changes along the Lowest-Triplet-State Path for C═C Bond Rotation of Annulenyl-Substituted Olefins Probed by the Electron Localization Function
inferred← citeshttps://doi.org/10.1021/ol401125fopenalex-snapshot
Dithieno[3,4-b:3′,4′-d]thiophene-Annelated Antiaromatic Planar Cyclooctatetraene with Olefinic Protons
inferred← citeshttps://doi.org/10.1021/om500545aopenalex-snapshot
Mechanistic Study of the Photochemical Isomerization Reactions of Silabenzene
inferred← citeshttps://doi.org/10.1038/nchem.1518openalex-snapshot
Exciting excited-state aromaticity
inferred← citeshttps://doi.org/10.1038/nchem.2233openalex-snapshot
Reversal of Hückel (anti)aromaticity in the lowest triplet states of hexaphyrins and spectroscopic evidence for Baird's rule
inferred← citeshttps://doi.org/10.1038/nchem.2242openalex-snapshot
A light-switched yin and yang pair
inferred← citeshttps://doi.org/10.1038/ncomms12962openalex-snapshot
Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
inferred← citeshttps://doi.org/10.1038/s41467-017-00382-1openalex-snapshot
Energetics of Baird aromaticity supported by inversion of photoexcited chiral [4n]annulene derivatives
inferred← citeshttps://doi.org/10.1038/s41467-019-10818-5openalex-snapshot
Non-aromatic annulene-based aggregation-induced emission system via aromaticity reversal process
inferred← citeshttps://doi.org/10.1038/s41467-019-12986-wopenalex-snapshot
Two-electron transfer stabilized by excited-state aromatization
inferred← citeshttps://doi.org/10.1039/c0cp02821eopenalex-snapshot
Influence of excited state aromaticity in the lowest excited singlet states of fulvene derivatives
inferred← citeshttps://doi.org/10.1039/c1cp22239bopenalex-snapshot
Electron delocalization and aromaticity in low-lying excited states of archetypal organic compounds
inferred← citeshttps://doi.org/10.1039/c1cp22415hopenalex-snapshot
Can an eight π-electron bare ring be planar?
inferred← citeshttps://doi.org/10.1039/c3cc41764fopenalex-snapshot
Antiaromatic planar cyclooctatetraene: a strategy for developing ambipolar semiconductors for field effect transistors
inferred← citeshttps://doi.org/10.1039/c4cp00860jopenalex-snapshot
Aromaticity of the planar hetero[8]circulenes and their doubly charged ions: NICS and GIMIC characterization
inferred← citeshttps://doi.org/10.1039/c4fd00084fopenalex-snapshot
A computational study of potential molecular switches that exploit Baird's rule on excited-state aromaticity and antiaromaticity
inferred← citeshttps://doi.org/10.1039/c4ra02693dopenalex-snapshot
The art of the possible: computational design of the 1D and 2D materials based on the tetraoxa[8]circulene monomer
inferred← citeshttps://doi.org/10.1039/c5cp00876jopenalex-snapshot
Influence of fluoro and cyano substituents in the aromatic and antiaromatic characteristics of cyclooctatetraene
inferred← citeshttps://doi.org/10.1039/c5cs00057bopenalex-snapshot
The excited state antiaromatic benzene ring: a molecular Mr Hyde?
inferred← citeshttps://doi.org/10.1039/c6cp08563fopenalex-snapshot
A new architecture for high spin organics based on Baird's rule of 4n electron triplet aromatics
inferred← citeshttps://doi.org/10.1039/c9cp02050kopenalex-snapshot
Demonstration of Baird's rule complementarity in the singlet state with implications for excited-state intramolecular proton transfer
inferred← citeshttps://doi.org/10.1039/c9cp06835jopenalex-snapshot
Design of annulene-within-an-annulene systems by the altanisation approach. A study of altan -[ n ]annulenes
inferred← citeshttps://doi.org/10.1039/d0cc02952aopenalex-snapshot
How does excited-state antiaromaticity affect the acidity strengths of photoacids?
inferred← citeshttps://doi.org/10.1039/d0cs01354dopenalex-snapshot
Heavier element-containing aromatics of [4 n +2]-electron systems
inferred← citeshttps://doi.org/10.1039/d0sc02294bopenalex-snapshot
Electron-driven proton transfer relieves excited-state antiaromaticity in photoexcited DNA base pairs
inferred← citeshttps://doi.org/10.1039/d1cc03701copenalex-snapshot
Magnetic shielding paints an accurate and easy-to-visualize portrait of aromaticity
inferred← citeshttps://doi.org/10.1039/d1cp04394copenalex-snapshot
Aromaticity reversals and their effect on bonding in the low-lying electronic states of cyclooctatetraene
inferred← citeshttps://doi.org/10.1039/d1cs00742dopenalex-snapshot
Porphyrinoids, a unique platform for exploring excited-state aromaticity
inferred← citeshttps://doi.org/10.1039/d1sc00382hopenalex-snapshot
Excited state character of Cibalackrot-type compounds interpreted in terms of Hückel-aromaticity: a rationale for singlet fission chromophore design
inferred← citeshttps://doi.org/10.1039/d3tc02151copenalex-snapshot
Triplet conformation in chromophore-fused cyclooctatetraene dyes
inferred← citeshttps://doi.org/10.1039/d4cp03198aopenalex-snapshot
Excited-state aromaticity reversals in norcorrole
inferred← citeshttps://doi.org/10.1039/d4ra05147eopenalex-snapshot
Aromatic stabilization energies in excited states at the multiconfigurational level: assessment in archetypal organic rings
inferred← citeshttps://doi.org/10.1039/d4sc00642aopenalex-snapshot
Excited-state antiaromaticity relief drives facile photoprotonation of carbons in aminobiphenyls
inferred← citeshttps://doi.org/10.1039/d4sc04692gopenalex-snapshot
Proton transfer induced excited-state aromaticity gain for chromophores with maximal Stokes shifts
inferred← citeshttps://doi.org/10.1039/d4sc07123aopenalex-snapshot
Stacked-ring aromaticity from the viewpoint of the effective number of π-electrons
inferred← citeshttps://doi.org/10.1039/d5cp03645copenalex-snapshot
Probing the stability of exocyclic BN-doped fulvenes in ground state: 1-aminoboroles vs. 1-pyrroloboranes
inferred← citeshttps://doi.org/10.1039/d6qo00375copenalex-snapshot
Auto-tandem palladium catalysis for unsymmetrical cyclooctatetraenes: modular synthesis and mechanistic elucidation
inferred← citeshttps://doi.org/10.1039/d6sc00969gopenalex-snapshot
Singlet machine learning photodynamics reveal competing inversion paths of methylated cyclooctatetrathiophene
inferred← citeshttps://doi.org/10.1063/1.3224127openalex-snapshot
Metal coordination converts the tub-shaped cyclo-octatetraene into an aromatic molecule: Electronic states and half-sandwich structures of group III metal-cyclo-octatetraene complexes
inferred← citeshttps://doi.org/10.1063/1.4801787openalex-snapshot
High-resolution electron spectroscopy of lanthanide (Ce, Pr, and Nd) complexes of cyclooctatetraene: The role of 4 f electrons
inferred← citeshttps://doi.org/10.1063/1.4812926openalex-snapshot
Communication: Two-determinant mixing with a strong-correlation density functional
inferred← citeshttps://doi.org/10.1070/rcr4445openalex-snapshot
Electronic structure, aromaticity and spectra of hetero[8]circulenes
inferred← citeshttps://doi.org/10.1080/00268976.2025.2451053openalex-snapshot
Excited state intramolecular proton transfer as a consequence of excited state aromaticity changes
inferred← citeshttps://doi.org/10.1246/bcsj.20160237openalex-snapshot
Graph Theory of Aromatic Stabilization
inferred← citeshttps://doi.org/10.1515/znb-2020-0024openalex-snapshot
The symmetry principle of antiaromaticity
inferred← citeshttps://doi.org/10.26434/chemrxiv-2023-w124bopenalex-snapshot
On-Surface Synthesis of a Doubly Anti-Aromatic Carbon Allotrope: Cyclo[16]carbon
inferred← citeshttps://doi.org/10.26434/chemrxiv.13498515openalex-snapshot
Guidelines for Tuning the Excited State Hückel-Baird Hybrid Aromatic Character of Pro-Aromatic Quinoidal Compounds
inferred← citeshttps://doi.org/10.26434/chemrxiv.13515989openalex-snapshot
Excited State Character of Cibalackrot-Type Compounds Interpreted in Terms of Hückel-Aromaticity: A Rational for Singlet Fission Chromophore Design
inferred← citeshttps://doi.org/10.3390/chemistry3030055openalex-snapshot
Singlet/Triplet State Anti/Aromaticity of CyclopentadienylCation: Sensitivity to Substituent Effect
inferred← citeshttps://doi.org/10.3390/chemistry3040102openalex-snapshot
Aromaticity of Heterocirculenes
inferred← citeshttps://doi.org/10.3390/chemistry7030079openalex-snapshot
Photocyclization of Alkenes and Arenes: Penetrating Through Aromatic Armor with the Help of Excited State Antiaromaticity
inferred← citeshttps://doi.org/10.3390/chemistry7040127openalex-snapshot
Aromaticity and Antiaromaticity: How to Define Them
inferred← citeshttps://doi.org/10.3390/inorganics5040091openalex-snapshot
The Silacyclobutene Ring: An Indicator of Triplet State Baird-Aromaticity
inferred← citeshttps://doi.org/10.3390/molecules25030711openalex-snapshot
How do the Hückel and Baird Rules Fade away in Annulenes?
inferred← citeshttps://doi.org/10.3390/molecules25204791openalex-snapshot
Are Multicentre Bond Indices and Related Quantities Reliable Predictors of Excited-State Aromaticity?
inferred← citeshttps://doi.org/10.3390/sym2010076openalex-snapshot
Recent Studies on the Aromaticity and Antiaromaticity of Planar Cyclooctatetraene
inferred← citeshttps://doi.org/10.3390/sym2031653openalex-snapshot
On the Importance of Clar Structures of Polybenzenoid Hydrocarbons as Revealed by the π-Contribution to the Electron Localization Function
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