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http://nopr.niscpr.res.in/handle/123456789/22442Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Singh, Harjit | - |
| dc.contributor.author | Sharma, Rajan | - |
| dc.contributor.author | Malik, Vaishalli | - |
| dc.contributor.author | Kumar, Subodh | - |
| dc.date.accessioned | 2013-10-22T10:51:00Z | - |
| dc.date.available | 2013-10-22T10:51:00Z | - |
| dc.date.issued | 2001-11 | - |
| dc.identifier.issn | 0975-0983(Online); 0376-4699(Print) | - |
| dc.identifier.uri | http://hdl.handle.net/123456789/22442 | - |
| dc.description | 1104-1107 | en_US |
| dc.description.abstract | The diesters 3 and 4 prepared by o-alkylations of 1,1'-bi-2-naphthol and 2,2' dihydroxybiphenyl with ethyl chloroacetate and the 1,3-diester of calix[4]arene undergo aminolysis with diethylenetriamine and 3,3'-diaminodipropylamine to provide dioxadiamide-amine based macrocycles. Amongst these macrocycles calix[4]arene based macrocycle 10 shows moderate selectivity towards Pb2+ over alkali and alkaline earth metal cations. | en_US |
| dc.language.iso | en_US | en_US |
| dc.publisher | NISCAIR-CSIR, India | en_US |
| dc.rights |  CC Attribution-Noncommercial-No Derivative Works 2.5 India | en_US |
| dc.source | IJC-B Vol.40B(11) [November 2001] | en_US |
| dc.title | Synthetic ionophores: Part 22 — Synthesis and ionophore behaviour of dioxadiamide-amine based macrocycles appended on binaphthol, biphenyl and calix[4]arene platforms† | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-B Vol.40B(11) [November 2001] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCB 40B(11) 1104-1107.pdf | 862.86 kB | Adobe PDF | View/Open |
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