Deeming, AJ and Hogarth, G and Lee, MYV and Saha, M and Redmond, SP and Phetmung, HT and Orpen, AG (2000) para-Ethynyl aniline as a building block for fully pi-conjugated ligands and acetylide complexes: crystal structures of trans-[Pt(PPh3)(2)(C CC6H4NH2)(2)] and [(mu-H)Ru-3(CO)(9)(mu(3)-C CC6H4NH2)]. INORG CHIM ACTA , 309 (1-2) 109 - 122.
Full text not available from this repository.
Abstract
para-Ethynyl aniline has been prepared, structurally characterised and investigated as a building block towards fully pi -conjugated multifunctional ligands and complexes. Palladium-copper catalysed coupling with aryl halides affords a number of new amino-substituted aryl acetylenes, while using [Ni(CO)(2)(PPh3)(2)] as a catalyst, cyclotrimerisation and dimerisation to give an ene-yne were competitive. Reaction of para-ethynyl aniline with low-valent metal centres affords acetylide complexes trans[Pt(PR3)(2)(C=CC6H4NH2)(2)] (R = Ph, Bu-n), cis-[Pt(eta (2)-dppe)(C=CC6H4NH2)(2)], all trans-[Ru(CO)(2)(PEt3)(2)(C=CC6H4NH2)(2)] and [(muH)Ru-3(CO)(9)(mu C-3=CC6H4NH2)]. The bis(acetylide) trans-[Pt(PPh3)(2)(C=CC6H4NH2)(2)] has been used to prepare extended chain complexes with amide, imine, imino-phosphorane and ferrocenyl imine units being generated. Attempts to prepare polymers via reaction with terephthaloyl chloride lead only to the formation of oligomers with an average of four monomer units. (C) 2000 Elsevier Science B.V. All rights reserved.
| Type: | Article |
|---|---|
| Title: | para-Ethynyl aniline as a building block for fully pi-conjugated ligands and acetylide complexes: crystal structures of trans-[Pt(PPh3)(2)(C CC6H4NH2)(2)] and [(mu-H)Ru-3(CO)(9)(mu(3)-C CC6H4NH2)] |
| Keywords: | acetylide, platinum complexes, pi-conjugated, anilines, X-RAY STRUCTURES, TERMINAL ALKYNES, SUBSTITUTED ACETYLENES, CATALYTIC ACTIVITY, CYCLOTRIMERIZATION, RUTHENIUM, OLIGOMERIZATION, PHENYLACETYLENE, NITROBENZENE, DIMERIZATION |
| UCL classification: | UCL > School of BEAMS > Faculty of Maths and Physical Sciences > Chemistry |
Archive Staff Only: edit this record