H/F isosteric substitution to attest different equi-energetic molecular conformations in crystals


Autoria(s): Dikundwar, Amol G; Venkateswarlu, Ch; Chandrakala, RN; Chandrasekaran, Srinivasan; Row, Tayur Guru N
Data(s)

2013

Resumo

The sequential replacement of aromatic H-atoms by F-atoms in 1,6-bis(phenylcarbonate) hexa-2,4-diyne allows access to its possible iso-energetic ``syn'', ``gauche'' and ``anti'' conformations.

Formato

application/pdf

Identificador

http://eprints.iisc.ernet.in/47082/1/CRYSTENGCOMM%20_15_27_5403_2013.pdf

Dikundwar, Amol G and Venkateswarlu, Ch and Chandrakala, RN and Chandrasekaran, Srinivasan and Row, Tayur Guru N (2013) H/F isosteric substitution to attest different equi-energetic molecular conformations in crystals. In: CRYSTENGCOMM, 15 (27). pp. 5403-5406.

Publicador

ROYAL SOC CHEMISTRY

Relação

http://dx.doi.org/ 10.1039/c3ce40697k

http://eprints.iisc.ernet.in/47082/

Palavras-Chave #Organic Chemistry #Solid State & Structural Chemistry Unit
Tipo

Journal Article

PeerReviewed