Acyclic Tetraethynylethene Molecular Scaffolding: Multinanometer-Sized Linearly Conjugated Rods with the Poly(triacetylene) Backbone and Cross-Conjugated Expanded Dendralenes

DOI: 10.1002/hlca.19950780402

Source and publish data:

Helvetica Chimica Acta p. 779 - 796 (1995)

Update date:2022-08-11

Topics:

Authors:

Boldi, Armen M.

Anthony, John

Gramlich, Volker

Knobler, Carolyn B.

Boudon, Corinne

et al. et al.

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Article abstract of DOI:10.1002/hlca.19950780402

Derivatives of fully cross-conjugated tetraethynylethene (3,4-diethynylhex-3-ene-1,5-diyne) 1 are versatile precursors to multinanometer-sized molecular rods with all-C-backbones.Oxidative polymerization (CuCl, N,N,N',N'-tetramethylethylenediamine (TMEDA)

Full text of DOI:10.1002/hlca.19950780402

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