Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/4828
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dc.coverage.spatialChemistryen_US
dc.date.accessioned2012-09-26T09:44:34Z-
dc.date.available2012-09-26T09:44:34Z-
dc.date.issued2012-09-26-
dc.identifier.urihttp://hdl.handle.net/10603/4828-
dc.description.abstractPART-I Hydrogen bonding patterns involving aminopyrimidine cocrystal/ salt interactions Chapter I Hydrogen bonding patterns in the co-crystal structures of 2-amino- 4,6 dimethoxypyrimidine-4-aminobenzoic acid [1/1] (1), 2-amino- 4,6-dimethoxypyrimidine-anthranilic acid [1/1] (2), 2-amino 4,6- dimethoxypyrimidine-phthalic acid [1/1] (3), 2-amino-4,6- dimethoxypyrimidine-2,4-dichlorobenzoic acid (1/1) (4) and 2- amino-4,6-dimethylpyrimidine-fumaric acid (0.5/0.5) (5) In all the compounds, the carboxylic acid group interacts with the corresponding 2-aminopyrimidine moiety through N-H?O and O-H?N hydrogen bonds to form an R22(8) ring motif. In compound 1, the R22(8) motif further self organizes through N-H?O hydrogen bonds to generate an array of six hydrogen bonds with rings having the graph-set notations R23(6), R22(8), R42(8), R22(8) and R23(6). The 4- aminobenzoic acid molecules self-assemble via N-H?O hydrogen bonds to form a supramolecular chain along the c-axis, with the graph-set notation C(9). In compound 2, inversion-related bases (molecules (AandB)) are paired via N(2)- H?N(3) hydrogen bonds forming another type of R22(8) motif. The carboxyl oxygen atom (O3A) of anthranilic acid (Molecule A) is linked to 4-amino group (N4B) of anthranilic acid (Molecule B) via N-H?O hydrogen bonds. In compound 3, the nitrogen atom (N3) and 2-amino (NH2) group of the pyrimidine ring also interact with carboxyl oxygen atoms (O5 and O6) to form an eight membered ring motif, generating a helical chain (made up of alternating pyrimidine and phthalic acid molecules) along the b-axis. This chain is interpenetrated by a centrosymmetrically related chain to which it is linked by and#61552;-and#61552; stacking of pyrimidines. In compound 4, the R22(8) motifs are centrosymmetrically paired via N-H?O hydrogen bonds to produce DADA (D-donor andA-acceptor) array of quadruple hydrogen bonds. The quadruple DADA arrays are further extended into ladders by pairs of C-H?O hydrogen bonds to form a R22(8) ring motif.en_US
dc.format.extent215p.en_US
dc.languageEnglishen_US
dc.relation215en_US
dc.rightsuniversityen_US
dc.titleCrystal structures of cocrystals/salts containing aminopyrimidines/aminotriazines: implications for crystal engineeringen_US
dc.title.alternative-en_US
dc.creator.researcherThanigaimani, Ken_US
dc.subject.keywordaminotriazinesen_US
dc.subject.keywordaminopyrimidinesen_US
dc.subject.keywordcrystal engineeringen_US
dc.subject.keywordSupramolecular Chemistryen_US
dc.description.noteReferences p.59-69en_US
dc.contributor.guideThomas Muthiah, Pen_US
dc.publisher.placeTiruchirappallien_US
dc.publisher.universityBharathidasan Universityen_US
dc.publisher.institutionDepartment of Chemistryen_US
dc.date.registeredn.d.en_US
dc.date.completedJune 2009en_US
dc.date.awarded2009en_US
dc.format.dimensions-en_US
dc.format.accompanyingmaterialNoneen_US
dc.type.degreePh.D.en_US
dc.source.inflibnetINFLIBNETen_US
Appears in Departments:Department of Chemistry

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01_title.pdfAttached File70.47 kBAdobe PDFView/Open
02_certificate.pdf23.58 kBAdobe PDFView/Open
03_declaration.pdf23.18 kBAdobe PDFView/Open
04_dedication.pdf46.39 kBAdobe PDFView/Open
05_abstract.pdf47.58 kBAdobe PDFView/Open
06_acknowledgements.pdf10.53 kBAdobe PDFView/Open
07_contents.pdf48.7 kBAdobe PDFView/Open
08_words.pdf10.06 kBAdobe PDFView/Open
09_introduction.pdf55.83 kBAdobe PDFView/Open
10_chapter 1.pdf101 kBAdobe PDFView/Open
11_chapter 2.pdf112.31 kBAdobe PDFView/Open
12_chapter 3.pdf66.28 kBAdobe PDFView/Open
13_chapter 4.pdf97.98 kBAdobe PDFView/Open
14_chapter 5.pdf78.47 kBAdobe PDFView/Open
15_chapter 6.pdf112.69 kBAdobe PDFView/Open
16_chapter 7.pdf89.52 kBAdobe PDFView/Open
17_references.pdf78.13 kBAdobe PDFView/Open
18_appendix.pdf1.46 MBAdobe PDFView/Open
19_list of publications.pdf10.56 kBAdobe PDFView/Open
20_figure, motifs and tables.pdf3.07 MBAdobe PDFView/Open


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