The Lewis electron-pair bonding model: the physical background, one century later

2019 ◽  
Vol 3 (1) ◽  
pp. 35-47 ◽  
Author(s):  
Lili Zhao ◽  
W. H. Eugen Schwarz ◽  
Gernot Frenking
2019 ◽  
Vol 55 (35) ◽  
pp. 5071-5074 ◽  
Author(s):  
J. Luis Casals-Sainz ◽  
F. Jiménez-Grávalos ◽  
E. Francisco ◽  
A. Martín Pendás

Charge-shift bonding (CSB) has been introduced as a distinct third family of electron-pair links that adds to the covalent and ionic tradition.


ChemInform ◽  
2010 ◽  
Vol 23 (38) ◽  
pp. no-no
Author(s):  
F. M. BICKELHAUPT ◽  
N. M. M. NIBBERING ◽  
E. M. VAN WEZENBEEK ◽  
E. J. BAERENDS

2014 ◽  
Vol 10 (6) ◽  
pp. 2410-2418 ◽  
Author(s):  
Huaiyu Zhang ◽  
David Danovich ◽  
Wei Wu ◽  
Benoît Braïda ◽  
Philippe C. Hiberty ◽  
...  

1992 ◽  
Vol 96 (12) ◽  
pp. 4864-4873 ◽  
Author(s):  
F. Matthias Bickelhaupt ◽  
Nico M. M. Nibbering ◽  
Egbert M. Van Wezenbeek ◽  
Evert Jan Baerends

Author(s):  
Sason Shaik ◽  
David Danovich ◽  
Benoit Braida ◽  
Wei Wu ◽  
Philippe C. Hiberty

2019 ◽  
Vol 3 (1) ◽  
pp. 48-63 ◽  
Author(s):  
Lili Zhao ◽  
Markus Hermann ◽  
W. H. Eugen Schwarz ◽  
Gernot Frenking

1991 ◽  
Vol 56 (10) ◽  
pp. 2160-2168 ◽  
Author(s):  
Josef Jirman

The 1H and 13C NMR spectra have been measured of six trans-azobenzenes substituted at 2 and 2’ positions with substituents favourable for complex formation with a metal (OH, NH2, NHCOCH3, COOH). From the standpoint of NMR such substituted trans-azobenzenes are present in solution in a rapid equilibrium following from rotation around the bond between C-1 of phenyl group and N atom of azo linkage. The predominant form has the substituent in the syn-position with respect to the free electron pair of the nearer azo nitrogen atom. The equilibrium is affected by dipolar aprotic solvents (such as hexadeuteriodimethyl sulfoxide) by decreasing the presence of the predominant form by 1 to 11%.


2020 ◽  
Vol 9 (1-2) ◽  
pp. 11-39 ◽  
Author(s):  
Stephan Gräf

AbstractThe use of ultra-short pulsed lasers enables the fabrication of laser-induced periodic surface structures (LIPSS) on various materials following a single-step, direct-writing technique. These specific, well-ordered nanostructures with periodicities in the order of the utilised laser wavelength facilitate the engineering of surfaces with functional properties. This review paper discusses the physical background of LIPSS formation on substrates with different material properties. Using the examples of structural colours, specific wetting states and the reduction of friction and wear, this work presents experimental approaches that allow to deliberately influence the LIPSS formation process and thus tailor the surface properties. Finally, the review concludes with some future developments and perspectives related to forthcoming applications of LIPSS-based surfaces are discussed.


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