Homologous Ladder Cyclohexasilanes

F Fan Fang (School of Science, Key Laboratory of High Performance Scientific Computation, Xihua University 1 , Chengdu 610039,) A Andrew Molino (Department of Chemistry) K Kelsie E. Wentz (Department of Chemistry, Johns Hopkins University, 3400 N. Charles St., Baltimore, Maryland 21218, United States) C Carlton P. Folster (Department of Chemistry Johns Hopkins University 3400 N. Charles St Baltimore Maryland 21218 USA) J Jessica L. Williams M Maxime A. Siegler (Department of Chemistry) R Rebekka S. Klausen (Department of Chemistry)

Abstract

Abstract We report the synthesis of five new examples of ladder cyclohexasilanes, possessing up to three consecutive fused rings and differing in relative ring fusion configuration and side chain structure. By coupling a 1,4‐dipotassiooligosilyl dianion to a cyclohexasilane, we obtained bi‐ and tricyclic ladder cyclohexasilanes. Combined experimental and theoretical studies suggested that annulation could favor the cis configuration under kinetic control, while the trans configuration predominates under thermodynamic control. Computational studies show that with each additional ring in the trans ‐diastereomeric series, the predicted onset of light absorption shifts to longer wavelengths.

Article Details

Volume / Issue Vol. 64, Issue 35
Published August 25, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (7)

F

Fan Fang

School of Science, Key Laboratory of High Performance Scientific Computation, Xihua University 1 , Chengdu 610039,

A

Andrew Molino

Department of Chemistry

K

Kelsie E. Wentz

Department of Chemistry, Johns Hopkins University, 3400 N. Charles St., Baltimore, Maryland 21218, United States

C

Carlton P. Folster

Department of Chemistry Johns Hopkins University 3400 N. Charles St Baltimore Maryland 21218 USA

J

Jessica L. Williams

M

Maxime A. Siegler

Department of Chemistry

R

Rebekka S. Klausen

Department of Chemistry