Efficient Synthetic Methods for the Installation of Boron-Nitrogen Bonds in Conjugated Organic Molecules

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dc.contributor.authorPiers, Warren E.
dc.contributor.authorMorgan, Matthew M.
dc.date.accessioned2016-04-13T07:48:27Z
dc.date.available2016-04-13T07:48:27Z
dc.date.issued2015-11-06
dc.descriptionAccepted version of article deposited April 11, 2016 as per http://www.rsc.org/journals-books-databases/journal-authors-reviewers/licences-copyright-permissions/#deposition-sharingen_US
dc.description.abstractPolycyclic aromatic hydrocarbons in which one or more CC units have been replaced by isoelectronic BN units have attracted interest as potentially improved organic materials in various devices. This promise has been hampered by a lack of access to gram quantities of these materials. However, the exploitation of keystone reactions such as ring closing metathesis, borylative cyclization of amino styrenes and electrophilic borylation has lead to strategies for access to workable amounts of material. These strategies can be augmented by judicious postfunctionalization reactions to diversify the library of materials available. This Frontier article highlights some of the recent successes and shows that the long promised applications of BN-doped PAHs are beginning to be explored in a meaningful way.en_US
dc.description.grantingagencyNSERCen_US
dc.description.refereedYesen_US
dc.identifier.citationDalton Trans., 2016, 45, 5920en_US
dc.identifier.doi10.1039/c5dt03991f
dc.identifier.doihttp://dx.doi.org/10.11575/PRISM/35408
dc.identifier.urihttp://hdl.handle.net/1880/51145
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.publisher.departmentChemistryen_US
dc.publisher.facultyScienceen_US
dc.publisher.institutionUniversity of Calgaryen_US
dc.publisher.urlhttp://pubs.rsc.org/en/Content/ArticleLanding/2016/DT/C5DT03991F#!divAbstracten_US
dc.titleEfficient Synthetic Methods for the Installation of Boron-Nitrogen Bonds in Conjugated Organic Moleculesen_US
dc.typejournal article
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