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Cited by 363

The DOI matches its Crossref record; 2 of the 2 references it cites were found in a registry or an index.

All‐Carbon Scaffolds by Rational Design

Diederich, François, Kivala, Milan·2010·Advanced Materials

Abstract

The search for new molecular and regular polymeric allotropes of carbon has greatly stimulated the preparation and investigation of π‐conjugated acetylenic macrocycles, which often represent substructures of proposed 2D carbon networks. Perethynylated dehydroannulenes, expanded radialenes, and radiaannulenes with large, multi‐nanometer‐sized all‐carbon cores are potent electron acceptors, and their optoelectronic as well as stability and solubility properties are greatly enhanced by peripheral donor substitution. Acetylenic scaffolding into three dimensions has generated an expanded cubane with a C 56 core, the first representative of a new class of “platonic” objects. Exceptional chiroptical properties displayed by enantiomerically pure alleno‐acetylenic, shape‐persistent macrocycles promise fascinating perspectives for the development of molecular and supramolecular chiroptical materials.

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Metadata

Authors
Diederich, F., & Kivala, M.
Venue
Advanced Materials
Publisher
Wiley
Published
2010-02-12
Volume
22
Issue
7
Pages
803-812
ISSN
  • 0935-9648 (ISSN-L)
  • 1521-4095
OpenAlex
W1987538906
Cited by
363
References
2
FWCI
6.07
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: All‐Carbon Scaffolds by Rational Design. https://app.cochat.ai/papers/10.1002/adma.200902623
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Diederich, F., & Kivala, M. (2010). All‐Carbon Scaffolds by Rational Design. Advanced Materials. https://doi.org/10.1002/adma.200902623

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