Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

Tetrel and pnictogen functionalised propargylidynes

dc.contributor.authorManzano, Richard
dc.contributor.authorHill, Anthony
dc.contributor.authorGeorgelin, Rosemary
dc.date.accessioned2020-12-13T22:57:37Z
dc.date.issued2020-12-04
dc.description.abstractThe reaction of [W([triple bond, length as m-dash]CC[triple bond, length as m-dash]CSiMe3)(CO)2(Tp*)] (Tp* = tris(dimethylpyrazolyl)borate) with AgNO3 affords {[W([triple bond, length as m-dash]CC[triple bond, length as m-dash]CAg)-(CO)2(Tp*)][AgNO3]}n while [Hg{C[triple bond, length as m-dash]CC[triple bond, length as m-dash]W(CO)2(Tp*)}2] with nBuLi affords [W([triple bond, length as m-dash]CC[triple bond, length as m-dash]CLi)(CO)2(Tp*)]. These anhydrous reagents allow the installation of main group elements (e.g., Si, Sn, Pb, P, As) as propargylidyne termini.en_AU
dc.description.sponsorshipDP170102695 and DP190100723en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1359-7345en_AU
dc.identifier.urihttp://hdl.handle.net/1885/216915
dc.language.isoen_AUen_AU
dc.provenancehttps://v2.sherpa.ac.uk/id/publication/18003..."The Accepted Version can be archived in a Non-Commercial Repository. 12 months embargo" from SHERPA/RoMEO site (as at 13/12/2020).en_AU
dc.publisherRoyal Society of Chemistryen_AU
dc.relationhttp://purl.org/au-research/grants/arc/DP170102695en_AU
dc.relationhttp://purl.org/au-research/grants/arc/DP190100723en_AU
dc.rights© Royal Society of Chemistry 2020en_AU
dc.sourceChemical communicationsen_AU
dc.titleTetrel and pnictogen functionalised propargylidynesen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue93en_AU
local.bibliographicCitation.lastpage14600en_AU
local.bibliographicCitation.startpage14597en_AU
local.contributor.affiliationManzano, R., Research Schoolof Chemistry, The Australian National Universityen_AU
local.contributor.affiliationHill, A., Research School of Chemistry, The Australian National Universityen_AU
local.contributor.affiliationGeorgelin, R. L., Research School of Chemistry, The Australian National Universityen_AU
local.contributor.authoruidu4030185en_AU
local.identifier.citationvolume56en_AU
local.identifier.doi10.1039/d0cc06196den_AU
local.identifier.essn1364-548Xen_AU
local.publisher.urlhttp://pubs.rsc.org/en/Journals/JournalIssues/CCen_AU
local.type.statusAccepted Versionen_AU

Downloads

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
10.1039_d0cc06196d.pdf
Size:
2.34 MB
Format:
Adobe Portable Document Format
Description:

License bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
license.txt
Size:
884 B
Format:
Item-specific license agreed upon to submission
Description: