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Facile Preparation of Organometallic Nanorods from Various Ethynyl‐Substituted Molecules
Author(s) -
Nishijo Junichi,
Akashi Takaaki,
Enomoto Masaya,
Akita Motoko
Publication year - 2019
Publication title -
chemistryopen
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.644
H-Index - 29
ISSN - 2191-1363
DOI - 10.1002/open.201900145
Subject(s) - phenylacetylene , nanorod , acetonitrile , chemistry , nanomaterials , molecule , aqueous solution , solvent , propyne , photochemistry , nanotechnology , organic chemistry , materials science , catalysis
A facile method to prepare one‐dimensional (1D) organometallic nanomaterials from various ethynyl‐substituted molecules is reported. The reactions of 3‐chloro‐1‐ethynylbenzene, p ‐ t Bu‐phenylacetylene and 4‐ethynylbiphenyl with Cu + ions in acetonitrile yield nanorod‐shaped copper acetylides (Cu−C≡C−R) crystals. In the case of linear alkynes, namely, propyne, 1‐pentyne and 1‐hexyne, it was found that using an aqueous ammonia/ethanol mixed solvent instead of acetonitrile is a better approach to obtain 1D nanostructures. This procedure also enables us to prepare functional 1D nanomaterials. We demonstrate the preparation of a paramagnetic nanorod from the organic radical p ‐ethynylphenyl nitronyl nitroxide, and fluorescent nanorods from 9‐ethynylphenanthrene and 2‐ethynyl‐9,9′‐spirobifluorene.

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