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http://nopr.niscpr.res.in/handle/123456789/46309Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Mishra, A | - |
| dc.contributor.author | Pandey, D S | - |
| dc.contributor.author | Mishra, K | - |
| dc.contributor.author | Agarwala, U C | - |
| dc.date.accessioned | 2019-03-20T11:06:06Z | - |
| dc.date.available | 2019-03-20T11:06:06Z | - |
| dc.date.issued | 1990-03 | - |
| dc.identifier.issn | 0975-0975(Online); 0376-4710(Print) | - |
| dc.identifier.uri | http://nopr.niscair.res.in/handle/123456789/46309 | - |
| dc.description | 251-254 | en_US |
| dc.description.abstract | Reactions between [RuC1L1L2(η5-C5H5)] (L1,L2 = PPh3, AsPh3 or SbPh3) or [RuCl L2(η5-C5H5)] [(L2, = 1,2-bis(diphenylphosphino)ethane (dppe) and 1,2-bis(diphenylphosphino)methane (dppm)]2 and l-ethynylpyrene [HC2R, R = pyrene], in the presence of NH4PF6, NaBF4 or NaBPh4, have given the corresponding cationic η'-vinylidene complexes. These cations are readily deprotonated to give the corresponding η'-ethynyl complexes. They have been characterised on the basis of elemental analyses and spectroscopic (IR, PMR and CMR) studies. The cationic and neutral products have been further treated with methanol and higher alcohols and the resulting products characterised. | 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-A Vol.29A(03) [March 1990] | en_US |
| dc.title | Reaction of 1-ethynylpyrene with cyclopentadienylruthenium complexes | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | IJC-A Vol.29A(03) [March 1990] | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| IJCA 29A(3) 251-254.pdf | 313.21 kB | Adobe PDF | View/Open |
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