Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/7701
Title: Dimer Formation in 4-Benzyl-5-Methoxymethyl-3-Methyl-1 H -Pyrrole-2-Carboxylic Acid Benzyl Ester
Authors: Silva, M. 
Sobral, A. 
Silva, J. 
Santos, A. 
Melo, S. 
Beja, A. 
Issue Date: 2007
Citation: Journal of Chemical Crystallography. 37:10 (2007) 695-698
Abstract: Abstract A new substituted pyrrole, a precursor of meso-free-porphyrins, has been synthesised and characterised by single-crystal X-ray diffraction: monoclinic, P21/c with a = 14.607(9) ?, b = 5.136(2) ?, c = 25.832(17) ?, ß = 108.14(5)?, Mr = 349.41, V = 1841.6(18) ?3, Z = 4. The molecules are assembled in centrosymmetric dimers via strong N–H...O hydrogen bonds. The dimers are gathered into chains via C–H...p intermolecular interactions. Graphical abstract The molecules in 4-benzyl-5-methoxymethyl-3-methyl-1H-pyrrole-2-carboxylic acid benzyl ester are joined in dimmers by strong hydrogen bonds. The dimmers are aggregated in chains running along the b axis through C-H...?€ intermoleculear interactions.
URI: http://hdl.handle.net/10316/7701
DOI: 10.1007/s10870-007-9234-5
Rights: openAccess
Appears in Collections:FCTUC Física - Artigos em Revistas Internacionais

Files in This Item:
File Description SizeFormat
obra.pdf260.28 kBAdobe PDFView/Open
Show full item record

SCOPUSTM   
Citations

11
checked on Feb 18, 2020

WEB OF SCIENCETM
Citations 5

11
checked on Oct 6, 2020

Page view(s)

204
checked on Jul 29, 2021

Download(s) 50

248
checked on Jul 29, 2021

Google ScholarTM

Check

Altmetric

Altmetric


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.