Substituent effects on the optical properties of naphthalenediimides: A frontier orbital analysis across the periodic table

2015 ◽  
Vol 37 (2) ◽  
pp. 304-313 ◽  
Author(s):  
Joshua R. Mulder ◽  
Célia Fonseca Guerra ◽  
J. Chris Slootweg ◽  
Koop Lammertsma ◽  
F. Matthias Bickelhaupt
Keyword(s):  
Optical Properties ◽  
Periodic Table ◽  
Substituent Effects ◽  
Frontier Orbital ◽  
Orbital Analysis

An MNDO study of sulfenium ions

1983 ◽  
Vol 61 (3) ◽  
pp. 589-593 ◽  
Author(s):  
Jack Leon Ginsburg ◽  
Richard Francis Langler
Keyword(s):  
Gas Phase ◽  
Substituent Effects ◽  
Frontier Orbital ◽  
Relative Stabilities ◽  
Ion Formation ◽  
Orbital Analysis

An MNDO study has been carried out on a variety of substituted sulfenium ions and sulfides. Relative stabilities in the gas phase have been calculated for several pairs of regioisomeric sulfenium ions. It is shown that sulfenium ions are stabilized by π-donors and that the substituent electronegativity is not an important factor. The potential implications of this result for the mechanism by which chlorosulfonium cations are converted into sulfenium ions in solution is discussed. Substituent effects on the energetics of sulfenium ion formation from sulfides have been obtained. It is shown that these effects also are related to the substituent's π-donating ability. A frontier-orbital analysis of selected sulfenium ions has been done and is discussed.

Substituent Effects on Optical Properties of Pyrrolizine-fused BOPYIN

2021 ◽  
pp. 119681
Author(s):  
Debao Liu ◽  
Liu Wen ◽  
Xi Chen ◽  
Jiaying Yan ◽  
Kaibo Zheng ◽  
...  
Keyword(s):  
Optical Properties ◽  
Substituent Effects

Theoretical studies on the optical properties and substituent effects of osmium (II) complexes Os(N^N)(CN)2(PH3)2

2008 ◽  
Vol 869 (1-3) ◽  
pp. 11-18
Author(s):  
Tao Liu ◽  
Bao-Hui Xia ◽  
Xin Zhou ◽  
Qing-Chuang Zheng ◽  
Qing-Jiang Pan ◽  
...  
Keyword(s):  
Optical Properties ◽  
Substituent Effects ◽  
Theoretical Studies

Properties of the [M(dppm)2M′]2+Building Blocks (M, M′ = Pd or Pt): Site Selectivity, Emission Features, and Frontier Orbital Analysis

2009 ◽  
Vol 48 (9) ◽  
pp. 4118-4133 ◽  
Author(s):  
Sébastien Clément ◽  
Shawkat M. Aly ◽  
Diana Bellows ◽  
Daniel Fortin ◽  
Carsten Strohmann ◽  
...  
Keyword(s):  
Building Blocks ◽  
Frontier Orbital ◽  
Site Selectivity ◽  
Orbital Analysis

Biodegradation Mechanism of Anionic Polyacrylamide in Coal Preparation Using Molecular Simulation

2021 ◽  
Author(s):  
Fanglue Wang ◽  
Dongchen Zhang ◽  
Xuefeng Wu ◽  
Shengsong Deng
Keyword(s):  
Hydrophobic Interactions ◽  
Interaction Mechanism ◽  
Docking Study ◽  
Binding Modes ◽  
Frontier Orbital ◽  
Orbital Theory ◽  
Orbital Analysis ◽  
Insight Into ◽  
Anionic Polyacrylamide ◽  
Rhodococcus Sp

Abstract Biodegradation of anionic polyacrylamide (HPAM) and polyacrylate (PAA) by key enzymes, such as amidase and bacterial laccase, have been reported. However, the interaction mechanism between HPAM or PAA and enzymes is still poorly unclear. Here, docking study was undertook to demonstrate the binding modes and interaction details for degradation of HPAM or PAA. Then, bioactivities between PAA and HPAM were compared with frontier orbital theory. The docking results showed that HPAM completely buried in pocket of Rhodococcus sp. N-771 amidase (Rh Amidase), while most of PAA molecule exposed outside pocket of Bacillus subtilis laccase ( B. subtilis laccase ), further suggesting PAA was much more difficult to degrade than HPAM. Hydrophobic interactions and hydrogen bonds were necessary for stabilizing HPAM-Rh Amidase or PAA- B. subtilis laccase complex. The frontier orbital analysis indicated that bioactivity of PAA was higher than that of PAA. These findings provide an insight into enzyme-catalyzed degradation of HPAM. It is helpful in designing highly efficient enzymes against HPAM or PAA to protect environment.

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