Source:http://linkedlifedata.com/resource/pubmed/id/12682411
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
Pt 4
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| pubmed:dateCreated |
2003-4-8
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| pubmed:abstractText |
Borohydride reduction of N-(4-nitrobenzylidene)-4-iodoaniline has yielded the title compound, 1,2-bis[4-(4-iodophenylaminomethyl)phenyl]diazene 1-oxide, C(26)H(22)I(2)N(4)O. The molecules lie across centres of inversion in P2(1)/c, with the azoxy O atom disordered over two sites, each having an occupancy of 0.5. The molecules are linked into sheets by a combination of C-H.O and C-H.pi(arene) hydrogen bonds.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
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| pubmed:month |
Apr
|
| pubmed:issn |
0108-2701
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| pubmed:author | |
| pubmed:issnType |
Print
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| pubmed:volume |
59
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
O207-9
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| pubmed:dateRevised |
2003-11-4
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| pubmed:year |
2003
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| pubmed:articleTitle |
4,4'-Bis(4-iodophenylaminomethyl)azoxybenzene: hydrogen-bonded sheets built from C--H.O and C--H...pi(arene) hydrogen bonds.
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| pubmed:affiliation |
School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST, Scotland. cg@st-andrews.ac.uk
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| pubmed:publicationType |
Journal Article
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