0000000001323419

AUTHOR

Guzmán L. Espejo

showing 5 related works from this author

Corrigendum: An Unusually Small Singlet-Triplet Gap in a Quinoidal 1,6-Methano[10]annulene Resulting from Baird's 4n π-Electron Triplet Stabilization.

2016

Within the continuum of π-extended quinoidal electronic structures exist molecules that by design can support open-shell diradical structures. The prevailing molecular design criteria for such structures involve proaromatic nature that evolves aromaticity in open-shell diradical resonance structures. A new diradical species built upon a quinoidal methano[10]annulene unit is synthesized and spectroscopically evaluated. The requisite intersystem crossing in the open-shell structure is accompanied by structural reorganization from a contorted Mobius aromatic-like shape in S0 to a more planar shape in the Huckel aromatic-like T1. This stability was attributed to Baird’s Rule which dictates the …

Intersystem crossingDiradicalChemical physicsChemistryExcited stateMoleculeAromaticityGeneral ChemistryElectronSinglet stateAnnulenePhotochemistryCatalysisAngewandte Chemie (International ed. in English)
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Diindeno-fusion of an anthracene as a design strategy for stable organic biradicals

2016

The consequence of unpaired electrons in organic molecules has fascinated and confounded chemists for over a century. The study of open-shell molecules has been rekindled in recent years as new synthetic methods, improved spectroscopic techniques and powerful computational tools have been brought to bear on this field. Nonetheless, it is the intrinsic instability of the biradical species that limits the practicality of this research. Here we report the synthesis and characterization of a molecule based on the diindeno[b,i]anthracene framework that exhibits pronounced open-shell character yet possesses remarkable stability. The synthetic route is rapid, efficient and possible on the gram sca…

Models MolecularChemical substanceFree RadicalsGeneral Chemical EngineeringChemistry OrganicElectronsCrystallography X-Ray010402 general chemistryPhotochemistry01 natural sciencesMagneticschemistry.chemical_compoundTriplet stateAnthracenesFusionAnthraceneMolecular StructureSpintronics010405 organic chemistryTemperatureGeneral Chemistry0104 chemical scienceschemistryPolycyclic HydrocarbonsScience technology and societyDerivative (chemistry)Nature Chemistry
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Innentitelbild: An Unusually Small Singlet-Triplet Gap in a Quinoidal 1,6-Methano[10]annulene Resulting from Baird’s 4nπ-Electron Triplet Stabilizati…

2015

ChemistryGeneral MedicineElectronSinglet stateAnnulenePhotochemistryAngewandte Chemie
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Inside Cover: An Unusually Small Singlet-Triplet Gap in a Quinoidal 1,6-Methano[10]annulene Resulting from Baird’s 4nπ-Electron Triplet Stabilization…

2015

ChemistryCover (algebra)AromaticityGeneral ChemistryElectronSinglet stateAnnulenePhotochemistryCatalysisAngewandte Chemie International Edition
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CCDC 1426708: Experimental Crystal Structure Determination

2016

Related Article: Gabriel E. Rudebusch, José L. Zafra, Kjell Jorner, Kotaro Fukuda, Jonathan L. Marshall, Iratxe Arrechea-Marcos, Guzmán L. Espejo, Rocío Ponce Ortiz, Carlos J. Gómez-García, Lev N. Zakharov, Masayoshi Nakano, Henrik Ottosson, Juan Casado, Michael M. Haley|2016|Nature Chemistry|8|753|doi:10.1038/nchem.2518

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters((816-dimesityldiindeno[12-b:1'2'-i]anthracene-614-diyl)diethyne-21-diyl)bis(triisopropylsilane)Experimental 3D Coordinates
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