Source:http://linkedlifedata.com/resource/pubmed/id/21123895
Subject | Predicate | Object | Context |
---|---|---|---|
pubmed-article:21123895 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:21123895 | lifeskim:mentions | umls-concept:C0027950 | lld:lifeskim |
pubmed-article:21123895 | lifeskim:mentions | umls-concept:C0071044 | lld:lifeskim |
pubmed-article:21123895 | lifeskim:mentions | umls-concept:C0047050 | lld:lifeskim |
pubmed-article:21123895 | lifeskim:mentions | umls-concept:C0205198 | lld:lifeskim |
pubmed-article:21123895 | pubmed:issue | Pt 12 | lld:pubmed |
pubmed-article:21123895 | pubmed:dateCreated | 2010-12-2 | lld:pubmed |
pubmed-article:21123895 | pubmed:abstractText | The structures of the anhydrous 1:1 proton-transfer compounds of isonipecotamide (piperidine-4-carboxamide) with picric acid and 3,5-dinitrosalicylic acid, namely 4-carbamoylpiperidinium 2,4,6-trinitrophenolate, C(6)H(13)N(2)O(+)·C(6)H(2)N(3)O(7)(-), (I), and 4-carbamoylpiperidinium 2-carboxy-4,6-dinitrophenolate [two forms of which were found, the monoclinic ?-polymorph, (II), and the triclinic ?-polymorph, (III)], C(6)H(13)N(2)O(+)·C(7)H(3)N(2)O(7)(-), have been determined at 200?K. All three compounds form hydrogen-bonded structures, viz. one-dimensional in (II), two-dimensional in (I) and three-dimensional in (III). In (I), the cations form centrosymmetric cyclic head-to-tail hydrogen-bonded homodimers [graph set R(2)(2)(14)] through lateral duplex piperidinium-amide N-H...O interactions. These dimers are extended into a two-dimensional network structure through further interactions with phenolate and nitro O-atom acceptors, including a direct symmetric piperidinium-phenol/nitro N-H...O,O cation-anion association [graph set R(1)(2)(6)]. The monoclinic polymorph, (II), has a similar R(1)(2)(6) cation-anion hydrogen-bonding interaction to (I) but with an additional conjoint symmetrical R(1)(2)(4) interaction as well as head-to-tail piperidinium-amide N-H...O,O hydrogen bonds and amide-carboxyl N-H...O hydrogen bonds, giving a network structure which includes large R(4)(3)(20) rings. The hydrogen bonding in the triclinic polymorph, (III), is markedly different from that of monoclinic (II). The asymmetric unit contains two independent cation-anion pairs which associate through cyclic piperidinium-carboxyl N-H...O,O' interactions [graph set R(1)(2)(4)]. The cations also show the zigzag head-to-tail piperidinium-amide N-H...O hydrogen-bonded chain substructures found in (II), but in addition feature amide-nitro and amide-phenolate N-H...O associations. As well, there is a centrosymmetric double-amide N-H...O(carboxyl) bridged bis(cation-anion) ring system [graph set R(4)(2)(8)] in the three-dimensional framework. The structures reported here demonstrate the utility of the isonipecotamide cation as a synthon with previously unrecognized potential for structure assembly applications. Furthermore, the structures of the two polymorphic 3,5-dinitrosalicylic acid salts show an unusual dissimilarity in hydrogen-bonding characteristics, considering that both were obtained from identical solvent systems. | lld:pubmed |
pubmed-article:21123895 | pubmed:language | eng | lld:pubmed |
pubmed-article:21123895 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:21123895 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:21123895 | pubmed:month | Dec | lld:pubmed |
pubmed-article:21123895 | pubmed:issn | 1600-5759 | lld:pubmed |
pubmed-article:21123895 | pubmed:author | pubmed-author:SmithGrahamG | lld:pubmed |
pubmed-article:21123895 | pubmed:author | pubmed-author:WermuthUrs... | lld:pubmed |
pubmed-article:21123895 | pubmed:issnType | Electronic | lld:pubmed |
pubmed-article:21123895 | pubmed:volume | 66 | lld:pubmed |
pubmed-article:21123895 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:21123895 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:21123895 | pubmed:pagination | o609-13 | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:meshHeading | pubmed-meshheading:21123895... | lld:pubmed |
pubmed-article:21123895 | pubmed:year | 2010 | lld:pubmed |
pubmed-article:21123895 | pubmed:articleTitle | Anhydrous 1:1 proton-transfer compounds of isonipecotamide with picric acid and 3,5-dinitrosalicylic acid: 4-carbamoylpiperidinium 2,4,6-trinitrophenolate and two polymorphs of 4-carbamoylpiperidinium 2-carboxy-4,6-dinitrophenolate. | lld:pubmed |
pubmed-article:21123895 | pubmed:affiliation | Faculty of Science and Technology, Queensland University of Technology, GPO Box 2434, Brisbane, Qld 4001, Australia. g.smith@qut.edu.au | lld:pubmed |
pubmed-article:21123895 | pubmed:publicationType | Journal Article | lld:pubmed |
pubmed-article:21123895 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |