H/F isosteric substitution to attest different equi-energetic molecular conformations in crystals
Data(s) |
2013
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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 |