Theoretical explanation of the low-lying ν6 vibrational fundamental of the FSO3 radical by the linear vibronic coupling approach

2013 ◽  
Vol 138 (23) ◽  
pp. 234307 ◽  
Author(s):  
Tereza Uhlíková ◽  
Štěpán Urban
Keyword(s):  
Theoretical Explanation ◽  
Vibronic Coupling ◽  
Coupling Approach

scholarly journals Analysis of the S2←S0 vibronic spectrum of the ortho-cyanophenol dimer using a multimode vibronic coupling approach

2015 ◽  
Vol 142 (8) ◽  
pp. 084308 ◽  
Author(s):  
Sabine Kopec ◽  
Philipp Ottiger ◽  
Samuel Leutwyler ◽  
Horst Köppel
Keyword(s):  
Vibronic Coupling ◽  
Vibronic Spectrum ◽  
Coupling Approach

Magnetic moments of multielectron mixed-valency dimer clusters in a dynamic intermediate vibronic coupling approach

1993 ◽  
Vol 34 (2) ◽  
pp. 184-190
Author(s):  
B. S. Tsukerblat ◽  
V. Ya. Gamurar' ◽  
A. V. Palii ◽  
G. M. Kishinevskaya ◽  
A. S. Berengol'ts
Keyword(s):  
Magnetic Moments ◽  
Vibronic Coupling ◽  
Mixed Valency ◽  
Coupling Approach

THE MULTI-MODE VIBRONIC-COUPLING APPROACH

2004 ◽  
pp. 323-367 ◽  
Author(s):  
Horst Köppel ◽  
Wolfgang Domcke ◽  
Lorenz S. Cederbaum
Keyword(s):  
Vibronic Coupling ◽  
Coupling Approach ◽  
Multi Mode

Glass transition for dipolar hard spheres: a mode-coupling approach

1998 ◽  
Vol 77 (2) ◽  
pp. 305-311 ◽  
Author(s):  
Thomas Scheidsteger, Rolf Schilling
Keyword(s):  
Glass Transition ◽  
Mode Coupling ◽  
Hard Spheres ◽  
Coupling Approach

Convergent Total Synthesis of Principinol D, a Rearranged Kaurane Diterpenoid

2019 ◽  
Author(s):  
Timothy Newhouse ◽  
Aneta Turlik ◽  
Yifeng Chen ◽  
Anthony Scruse
Keyword(s):  
Total Synthesis ◽  
Natural Product ◽  
Late Stage ◽  
Membered Ring ◽  
Entry Point ◽  
Ketone Reduction ◽  
Coupling Approach

<div> <p>The total synthesis of principinol D, a rearranged kaurane diterpenoid, is reported. This grayanane natural product is constructed via a convergent fragment coupling approach, wherein the central 7-membered ring is synthesized at a late stage. The bicyclo[3.2.1]octane fragment is accessed by a Ni-catalyzed α-vinylation reaction. Strategic reductions include a diastereoselective SmI<sub>2</sub>-mediated ketone reduction with PhSH and a new protocol for selective ester reduction in the presence of ketones. The convergent strategy reported herein may be an entry point to the larger class of kaurane diterpenoids.</p> </div>

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