Articles with "conjugated macrocycles" as a keyword



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Porphyriynes: 18-π-Conjugated Macrocycles Incorporating a Triple Bond.

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Published in 2022 at "Organic letters"

DOI: 10.1021/acs.orglett.2c00356

Abstract: Tetraphenylporphyriyne (Pyne1), a novel porphyrin analogue with a C≡C bond incorporated into an 18-π-conjugated system, has been created via cleavage of the N-confused pyrrolic ring in Ag(III) N-confused tetraphenylporphyrin. The structure of Pyne1 was confirmed… read more here.

Keywords: conjugated macrocycles; incorporating triple; macrocycles incorporating; porphyriynes conjugated ... See more keywords
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Three-Dimensional Fully π-Conjugated Macrocycles: When 3D-Aromatic and When 2D-Aromatic-in-3D?

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Published in 2022 at "Journal of the American Chemical Society"

DOI: 10.1021/jacs.1c13478

Abstract: Several fully π-conjugated macrocycles with puckered or cage-type structures were recently found to exhibit aromatic character according to both experiments and computations. We examine their electronic structures and put them in relation to 3D-aromatic molecules… read more here.

Keywords: conjugated macrocycles; electron counts; three dimensional; aromatic aromatic ... See more keywords
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Oxidative insertion of amines into conjugated macrocycles: transformation of antiaromatic norcorrole into aromatic azacorrole.

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Published in 2023 at "Chemical communications"

DOI: 10.1039/d2cc06648c

Abstract: A new group of aromatic porphyrinoids was obtained by an oxidative insertion of primary amines into the antiaromatic ring of 5,14-dimesityl-norcorrolatonickel(II) activated by iodosobenzene. The substituted 10-azacorroles thus formed were characterized by spectroscopic and electrochemical… read more here.

Keywords: conjugated macrocycles; macrocycles transformation; insertion amines; amines conjugated ... See more keywords
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From luminescent π-conjugated macrocycles to bridged multi-cyclic π-conjugated polymers: cyclic topology, aggregation-induced emission and explosive sensing

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Published in 2023 at "Polymer Chemistry"

DOI: 10.1039/d3py00298e

Abstract: Topology is a unique dimension for macromolecular engineering, which has continuously spurred the creativity in the synthetic chemistry to explore the boundary of possible topology and architecture adopted by polymers.... read more here.

Keywords: topology; luminescent conjugated; conjugated macrocycles; chemistry ... See more keywords
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The Synthesis, Properties, and Application of o-Carborane-based π-Conjugated Macrocycles

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Published in 2023 at "Organic Chemistry Frontiers"

DOI: 10.1039/d3qo00487b

Abstract: Two o-carborane-based π-conjugated macrocycles are synthesized via oxidative coupling of acetylene-terminated o-carborane precursors. The single-crystal X-ray diffraction analysis unambiguously revealed their unique porous supramolecular structures, which display micropore characteristics. The... read more here.

Keywords: conjugated macrocycles; carborane based; properties application; carborane ... See more keywords