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DC Field | Value | Language |
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dc.contributor.author | Haridas, V | - |
dc.contributor.author | Sandhya, S | - |
dc.contributor.author | Geeta, H | - |
dc.contributor.author | Suresh, C H | - |
dc.date.accessioned | 2013-06-17T08:06:47Z | - |
dc.date.available | 2013-06-17T08:06:47Z | - |
dc.date.issued | 2012-10-10 | - |
dc.identifier.citation | Tetrahedron Letters 53(41):5523-5527;10 Oct 2012 | en_US |
dc.identifier.uri | http://hdl.handle.net/123456789/467 | - |
dc.description.abstract | Amino acid-based molecules containing a bis-urea moiety have been synthesized and demonstrated for their anion binding affinities. Compound 1c binds phosphate and sulfate with binding constants of 3.6 103 M 1 and 4.3 103 M 1, respectively. These molecules undergo proton transfer upon treatment with fluoride, resulting in the formation of imidazolidinediones. The crystal structure of one such diimidazolidinedione displays self-assembly through nonconventional hydrogen bonding interactions | en_US |
dc.language.iso | en | en_US |
dc.publisher | Elsevier | en_US |
dc.subject | Receptors | en_US |
dc.subject | Urea | en_US |
dc.subject | Anions | en_US |
dc.subject | Cyclization | en_US |
dc.subject | Imidazolidinedione | en_US |
dc.title | 1,3-Phenyl linked urea-based receptors for anions and the facile cyclization to imidazolidinedione | en_US |
dc.type | Article | en_US |
niist.citation | - | |
Appears in Collections: | 2012 |
Files in This Item:
File | Description | Size | Format | |
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2012 _0101.pdf Restricted Access | 808.36 kB | Adobe PDF | View/Open Request a copy |
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