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Front Cover: Intense Molar Circular Dichroism in Fully Conjugated All‐Carbon Macrocyclic 1,3‐Butadiyne Linked pseudo‐meta [2.2]Paracyclophanes (Chem. Eur. J. 53/2022).

Authors :
Sidler, Eric
Zwick, Patrick
Kress, Charlotte
Reznikova, Ksenia
Fuhr, Olaf
Fenske, Dieter
Mayor, Marcel
Source :
Chemistry - A European Journal. 9/22/2022, Vol. 28 Issue 53, p1-1. 1p.
Publication Year :
2022

Abstract

Front Cover: Intense Molar Circular Dichroism in Fully Conjugated All-Carbon Macrocyclic 1,3-Butadiyne Linked pseudo-meta [2.2]Paracyclophanes (Chem. Eur. J. 53/2022) The angle and flexibility of the pseudo- I meta i substituents enabled high yielding macrocyclization reactions, and the studied trimeric, tetrameric, pentameric and hexameric structures further displayed astonishing through-space polymer-like conjugation lengths. Keywords: [2.2]paracyclophane; hydrocarbon; macrocycle; molar circular dichroism; -conjugation EN [2.2]paracyclophane hydrocarbon macrocycle molar circular dichroism -conjugation 1 1 1 09/27/22 20220922 NES 220922 B Unprecedented high molar circular b dichroism values for all-carbon macrocycles were revealed in 1,3-butadiyne bridged pseudo- I meta- i [2.2]paracyclophanes. [Extracted from the article]

Details

Language :
English
ISSN :
09476539
Volume :
28
Issue :
53
Database :
Academic Search Index
Journal :
Chemistry - A European Journal
Publication Type :
Academic Journal
Accession number :
159294991
Full Text :
https://doi.org/10.1002/chem.202202705