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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).
- 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]
- Subjects :
- CIRCULAR dichroism
PARACYCLOPHANES
Subjects
Details
- Language :
- English
- ISSN :
- 09476539
- Volume :
- 28
- Issue :
- 53
- Database :
- Complementary Index
- Journal :
- Chemistry - A European Journal
- Publication Type :
- Academic Journal
- Accession number :
- 159294991
- Full Text :
- https://doi.org/10.1002/chem.202202705