(\pi\)-Radical Formation by Pyrrolic H Abstraction of Phthalocyanine Molecules on Molybdenum Disulfi...
(\pi\)-Radical Formation by Pyrrolic H Abstraction of Phthalocyanine Molecules on Molybdenum Disulfide
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Ithaca: Cornell University Library, arXiv.org
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English
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Ithaca: Cornell University Library, arXiv.org
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For a molecular radical to be stable, the environment needs to be inert. Furthermore, an unpaired electron is less likely to react chemically, when it is placed in an extended orbital. Here, we use the tip of a scanning tunneling microscope to abstract one of the pyrrolic hydrogen atoms from phthalocyanine (H2Pc) deposited on a single layer of moly...
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(\pi\)-Radical Formation by Pyrrolic H Abstraction of Phthalocyanine Molecules on Molybdenum Disulfide
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TN_cdi_proquest_journals_2234277475
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_2234277475
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2331-8422
DOI
10.48550/arxiv.1905.13692
