Conformational analysis of methyl-substituted 9,10-dihydroanthracenes

Gianfranco Fontana; Gianfranco La Manna; Maria Concetta Natoli

Conformational analysis of methyl-substituted 9,10-dihydroanthracenes

Gianfranco Fontana, Gianfranco La Manna, Maria Concetta Natoli

Scienze e Tecnologie Biologiche Chimiche e Farmaceutiche

Risultato della ricerca: Article › peer review

1 Citazioni (Scopus)

Abstract

The amount of the ring puckering in methyl-substituted 9,10- dihydroanthracene was theoretically determined through DFT calculations. Theoretical calculations allowed to obtain the geometrical structures and energetic data on the different considered isomers.

Lingua originale	English
pagine (da-a)	41-45
Numero di pagine	5
Rivista	JOURNAL OF MOLECULAR STRUCTURE. THEOCHEM
Volume	719
Stato di pubblicazione	Published - 2005

All Science Journal Classification (ASJC) codes

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???subjectarea.asjc.3100.3104???
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title = "Conformational analysis of methyl-substituted 9,10-dihydroanthracenes",

abstract = "The amount of the ring puckering in methyl-substituted 9,10- dihydroanthracene was theoretically determined through DFT calculations. Theoretical calculations allowed to obtain the geometrical structures and energetic data on the different considered isomers.",

author = "Gianfranco Fontana and {La Manna}, Gianfranco and Natoli, {Maria Concetta}",

year = "2005",

language = "English",

volume = "719",

pages = "41--45",

journal = "Journal of Molecular Structure: THEOCHEM",

issn = "0166-1280",

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T1 - Conformational analysis of methyl-substituted 9,10-dihydroanthracenes

AU - Fontana, Gianfranco

AU - La Manna, Gianfranco

AU - Natoli, Maria Concetta

PY - 2005

Y1 - 2005

N2 - The amount of the ring puckering in methyl-substituted 9,10- dihydroanthracene was theoretically determined through DFT calculations. Theoretical calculations allowed to obtain the geometrical structures and energetic data on the different considered isomers.

AB - The amount of the ring puckering in methyl-substituted 9,10- dihydroanthracene was theoretically determined through DFT calculations. Theoretical calculations allowed to obtain the geometrical structures and energetic data on the different considered isomers.

UR - http://hdl.handle.net/10447/30085

M3 - Article

VL - 719

SP - 41

EP - 45

JO - Journal of Molecular Structure: THEOCHEM

JF - Journal of Molecular Structure: THEOCHEM

SN - 0166-1280

ER -

Conformational analysis of methyl-substituted 9,10-dihydroanthracenes

Abstract

All Science Journal Classification (ASJC) codes

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