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http://hdl.handle.net/10603/4828
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DC Field | Value | Language |
---|---|---|
dc.coverage.spatial | Chemistry | en_US |
dc.date.accessioned | 2012-09-26T09:44:34Z | - |
dc.date.available | 2012-09-26T09:44:34Z | - |
dc.date.issued | 2012-09-26 | - |
dc.identifier.uri | http://hdl.handle.net/10603/4828 | - |
dc.description.abstract | PART-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.extent | 215p. | en_US |
dc.language | English | en_US |
dc.relation | 215 | en_US |
dc.rights | university | en_US |
dc.title | Crystal structures of cocrystals/salts containing aminopyrimidines/aminotriazines: implications for crystal engineering | en_US |
dc.title.alternative | - | en_US |
dc.creator.researcher | Thanigaimani, K | en_US |
dc.subject.keyword | aminotriazines | en_US |
dc.subject.keyword | aminopyrimidines | en_US |
dc.subject.keyword | crystal engineering | en_US |
dc.subject.keyword | Supramolecular Chemistry | en_US |
dc.description.note | References p.59-69 | en_US |
dc.contributor.guide | Thomas Muthiah, P | en_US |
dc.publisher.place | Tiruchirappalli | en_US |
dc.publisher.university | Bharathidasan University | en_US |
dc.publisher.institution | Department of Chemistry | en_US |
dc.date.registered | n.d. | en_US |
dc.date.completed | June 2009 | en_US |
dc.date.awarded | 2009 | en_US |
dc.format.dimensions | - | en_US |
dc.format.accompanyingmaterial | None | en_US |
dc.type.degree | Ph.D. | en_US |
dc.source.inflibnet | INFLIBNET | en_US |
Appears in Departments: | Department of Chemistry |
Files in This Item:
File | Description | Size | Format | |
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01_title.pdf | Attached File | 70.47 kB | Adobe PDF | View/Open |
02_certificate.pdf | 23.58 kB | Adobe PDF | View/Open | |
03_declaration.pdf | 23.18 kB | Adobe PDF | View/Open | |
04_dedication.pdf | 46.39 kB | Adobe PDF | View/Open | |
05_abstract.pdf | 47.58 kB | Adobe PDF | View/Open | |
06_acknowledgements.pdf | 10.53 kB | Adobe PDF | View/Open | |
07_contents.pdf | 48.7 kB | Adobe PDF | View/Open | |
08_words.pdf | 10.06 kB | Adobe PDF | View/Open | |
09_introduction.pdf | 55.83 kB | Adobe PDF | View/Open | |
10_chapter 1.pdf | 101 kB | Adobe PDF | View/Open | |
11_chapter 2.pdf | 112.31 kB | Adobe PDF | View/Open | |
12_chapter 3.pdf | 66.28 kB | Adobe PDF | View/Open | |
13_chapter 4.pdf | 97.98 kB | Adobe PDF | View/Open | |
14_chapter 5.pdf | 78.47 kB | Adobe PDF | View/Open | |
15_chapter 6.pdf | 112.69 kB | Adobe PDF | View/Open | |
16_chapter 7.pdf | 89.52 kB | Adobe PDF | View/Open | |
17_references.pdf | 78.13 kB | Adobe PDF | View/Open | |
18_appendix.pdf | 1.46 MB | Adobe PDF | View/Open | |
19_list of publications.pdf | 10.56 kB | Adobe PDF | View/Open | |
20_figure, motifs and tables.pdf | 3.07 MB | Adobe PDF | View/Open |
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