ChemInform Abstract: FAILURES OF THE TOPOLOGICAL RESONANCE ENERGY METHOD

1980 ◽  
Vol 11 (44) ◽  
Author(s):  
I. GUTMAN
Keyword(s):  
Energy Method ◽  
Resonance Energy ◽  
Topological Resonance Energy

scholarly journals A study on the aromatic conjugation pathways and the ring currents of bridged [18]annulenes

RSC Advances ◽  
2019 ◽  
Vol 9 (44) ◽  
pp. 25351-25357
Author(s):  
Qimanguli Tuoheti ◽  
Ablikim Kerim
Keyword(s):  
Energy Method ◽  
Resonance Energy ◽  
Hydrogen Atoms ◽  
Ring Currents ◽  
Topological Resonance Energy

The topological resonance energy method was used to investigate the global aromaticity of a set of [18]annulene-derived compounds obtained by replacing two, four, or all six of the inner hydrogen atoms with bridges (oxygen, imino-, sulfur, or combinations of the three).

A regularity in Herndon's resonance energy method

1985 ◽  
Vol 115 (4-5) ◽  
pp. 416-418 ◽  
Author(s):  
Ivan Gutman ◽  
Sherif El-Basil
Keyword(s):  
Energy Method ◽  
Resonance Energy

The Cycle-Dependence of Topological Resonance Energy.

ChemInform ◽  
2007 ◽  
Vol 38 (33) ◽  
Author(s):  
Ivan Gutman ◽  
Sonja Stankovic ◽  
Jelena Durdevic ◽  
Boris Furtula
Keyword(s):  
Resonance Energy ◽  
Topological Resonance Energy ◽  
Cycle Dependence

A concealed difference between the structure-dependence of Dewar and topological resonance energy

2005 ◽  
Vol 757 (1-3) ◽  
pp. 119-123 ◽  
Author(s):  
Ivan Gutman ◽  
Sabina Gojak ◽  
Sonja Stanković ◽  
Boris Furtula
Keyword(s):  
Resonance Energy ◽  
Structure Dependence ◽  
Topological Resonance Energy

Delocalization and stability of o- and p-quinone methides: A HMO study

1981 ◽  
Vol 46 (5) ◽  
pp. 1148-1159 ◽  
Author(s):  
Lubomír Musil ◽  
Bohumír Koutek ◽  
Milena Píšová ◽  
Milan Souček
Keyword(s):  
Resonance Energy ◽  
Quinone Methides ◽  
Nucleophilic Reactivity ◽  
Topological Resonance Energy

A series of twenty one p- and o-quinone methides has been investigated by the HMO method. Stability predictions for compounds I-XIII are based on a combination of their topological resonance energy, nucleophilic reactivity and dimerization ability. The obtained results have been verified by the synthesis of four new quinone methides IIb, Vb, VIa and VIb.

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