Linked Life Data

17944502

Source:http://linkedlifedata.com/resource/pubmed/id/17944502

Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
24
pubmed:dateCreated
2007-11-13
pubmed:abstractText
Integrated studies using scanning tunneling microscopy and X-ray crystallography have established that 4,5,9,10-tetrahydropyrene-2,7-dicarboxylic acid and pyrene-2,7-dicarboxylic acid crystallize in 2D and 3D with striking homology. Different behavior is shown by related biphenyls that lack the planarizing conformational constraints of the pyrenyl core and the directing effects of intermolecular hydrogen bonding. The results of these studies show that molecules specifically designed to engage in multiple strong directional interadsorbate interactions are promising tools for imposing particular nanopatterns on surfaces and for revealing subtle aspects of crystallization.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Nov
pubmed:issn
0743-7463
pubmed:author
pubmed:issnType
Print
pubmed:day
20
pubmed:volume
23
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
11980-5
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
Ensuring homology between 2D and 3D molecular crystals.
pubmed:affiliation
Département de Chimie and Faculté de Médecine Dentaire, Université de Montréal, Montréal, Québec, Canada. dang@chem.ucla.edu
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't