Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene

Baird’s rules say that the first triplet state of benzene displays antiaromatic character. Here, the authors exploit this to show that aromatic molecules can undergo rapid transfer hydrogenation or silylations without the need for metal catalysts when photochemcially excited into this state.

Guardado en:
Detalles Bibliográficos
Autores principales: Raffaello Papadakis, Hu Li, Joakim Bergman, Anna Lundstedt, Kjell Jorner, Rabia Ayub, Soumyajyoti Haldar, Burkhard O. Jahn, Aleksandra Denisova, Burkhard Zietz, Roland Lindh, Biplab Sanyal, Helena Grennberg, Klaus Leifer, Henrik Ottosson
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2016
Materias:
Q
Acceso en línea:https://doaj.org/article/22c966a83af84406bcc41b47bcd48edd
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:22c966a83af84406bcc41b47bcd48edd
record_format dspace
spelling oai:doaj.org-article:22c966a83af84406bcc41b47bcd48edd2021-12-02T14:39:32ZMetal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene10.1038/ncomms129622041-1723https://doaj.org/article/22c966a83af84406bcc41b47bcd48edd2016-10-01T00:00:00Zhttps://doi.org/10.1038/ncomms12962https://doaj.org/toc/2041-1723Baird’s rules say that the first triplet state of benzene displays antiaromatic character. Here, the authors exploit this to show that aromatic molecules can undergo rapid transfer hydrogenation or silylations without the need for metal catalysts when photochemcially excited into this state.Raffaello PapadakisHu LiJoakim BergmanAnna LundstedtKjell JornerRabia AyubSoumyajyoti HaldarBurkhard O. JahnAleksandra DenisovaBurkhard ZietzRoland LindhBiplab SanyalHelena GrennbergKlaus LeiferHenrik OttossonNature PortfolioarticleScienceQENNature Communications, Vol 7, Iss 1, Pp 1-10 (2016)
institution DOAJ
collection DOAJ
language EN
topic Science
Q
spellingShingle Science
Q
Raffaello Papadakis
Hu Li
Joakim Bergman
Anna Lundstedt
Kjell Jorner
Rabia Ayub
Soumyajyoti Haldar
Burkhard O. Jahn
Aleksandra Denisova
Burkhard Zietz
Roland Lindh
Biplab Sanyal
Helena Grennberg
Klaus Leifer
Henrik Ottosson
Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
description Baird’s rules say that the first triplet state of benzene displays antiaromatic character. Here, the authors exploit this to show that aromatic molecules can undergo rapid transfer hydrogenation or silylations without the need for metal catalysts when photochemcially excited into this state.
format article
author Raffaello Papadakis
Hu Li
Joakim Bergman
Anna Lundstedt
Kjell Jorner
Rabia Ayub
Soumyajyoti Haldar
Burkhard O. Jahn
Aleksandra Denisova
Burkhard Zietz
Roland Lindh
Biplab Sanyal
Helena Grennberg
Klaus Leifer
Henrik Ottosson
author_facet Raffaello Papadakis
Hu Li
Joakim Bergman
Anna Lundstedt
Kjell Jorner
Rabia Ayub
Soumyajyoti Haldar
Burkhard O. Jahn
Aleksandra Denisova
Burkhard Zietz
Roland Lindh
Biplab Sanyal
Helena Grennberg
Klaus Leifer
Henrik Ottosson
author_sort Raffaello Papadakis
title Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
title_short Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
title_full Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
title_fullStr Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
title_full_unstemmed Metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
title_sort metal-free photochemical silylations and transfer hydrogenations of benzenoid hydrocarbons and graphene
publisher Nature Portfolio
publishDate 2016
url https://doaj.org/article/22c966a83af84406bcc41b47bcd48edd
work_keys_str_mv AT raffaellopapadakis metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT huli metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT joakimbergman metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT annalundstedt metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT kjelljorner metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT rabiaayub metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT soumyajyotihaldar metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT burkhardojahn metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT aleksandradenisova metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT burkhardzietz metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT rolandlindh metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT biplabsanyal metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT helenagrennberg metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT klausleifer metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
AT henrikottosson metalfreephotochemicalsilylationsandtransferhydrogenationsofbenzenoidhydrocarbonsandgraphene
_version_ 1718390580958986240