| dc.contributor.author | DRAPER, SYLVIA MARY | en |
| dc.date.accessioned | 2014-01-28T11:53:12Z | |
| dc.date.available | 2014-01-28T11:53:12Z | |
| dc.date.issued | 2011 | en |
| dc.date.submitted | 2011 | en |
| dc.identifier.citation | Martin C.J., Gil B., Draper S.M., Thienyl directed polyaromatic C-C bond fusions: S-doped hexabenzocoronenes, Chemical Communications, 47, 12, 2011, 3616 - 3618 | en |
| dc.identifier.other | Y | en |
| dc.description | PUBLISHED | en |
| dc.description.abstract | With a view to combining the desirable electronic and
photochemical properties of hexabenzocoronene (HBC) and
the C?C bond forming capabilities of thiophenes, 1-(3-thienyl)-
2,3,4,5,6-penta(4-
tert
-butyl-phenyl)benzene (1) was oxidised
using FeCl
3
. The resulting products, superaromatic thiophene
(2) and its 5,5
0
-dimer (3), are S-HBC systems and provide a new
pair of spectral comparators | en |
| dc.format.extent | 3616 | en |
| dc.format.extent | 3618 | en |
| dc.language.iso | en | en |
| dc.relation.ispartofseries | Chemical Communications | en |
| dc.relation.ispartofseries | 47 | en |
| dc.relation.ispartofseries | 12 | en |
| dc.rights | Y | en |
| dc.subject | Chemistry | en |
| dc.title | Thienyl directed polyaromatic C-C bond fusions: S-doped hexabenzocoronenes | en |
| dc.type | Journal Article | en |
| dc.type.supercollection | scholarly_publications | en |
| dc.type.supercollection | refereed_publications | en |
| dc.identifier.peoplefinderurl | http://people.tcd.ie/smdraper | en |
| dc.identifier.rssinternalid | 70991 | en |
| dc.rights.ecaccessrights | OpenAccess | |
| dc.identifier.uri | http://hdl.handle.net/2262/67918 | |
