| Makale Türü | Özgün Makale (SSCI, AHCI, SCI, SCI-Exp dergilerinde yayınlanan tam makale) | ||
| Dergi Adı | Journal of Biological Inorganic Chemistry (Q2) | ||
| Dergi ISSN | 0949-8257 Wos Dergi Scopus Dergi | ||
| Dergi Tarandığı Indeksler | SCI-Expanded | ||
| Makale Dili | İngilizce | Basım Tarihi | 01-2015 |
| Kabul Tarihi | – | Yayınlanma Tarihi | 10-12-2014 |
| Cilt / Sayı / Sayfa | 20 / 1 / 165–178 | DOI | 10.1007/s00775-014-1223-5 |
| Makale Linki | http://link.springer.com/10.1007/s00775-014-1223-5 | ||
| UAK Araştırma Alanları |
Anorganik Kimya
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| Özet |
| The gradual Cl replacement reactions of NN (1–3) or NO spirocyclic monoferrocenyl cyclotriphosphazenes (4 and 5) with the potassium salt of 4-hydroxy-3-methoxybenzaldehyde (potassium vanillinate) resulted in the mono (1a–5a), geminal (gem-1b–5b), non-geminal (cis-5b and trans-1b–4b), tri (1c, 3c–5c) and tetra-vanillinato-substituted phosphazenes (1d–5d). All the phosphazene derivatives have stereogenic P-center(s), except tetra-substituted ones. The vanillinatophosphazenes have reversible voltammograms with one-electron anodic and cathodic peaks which are attributed to ferrocenyl redox probe. The structures of the new phosphazene compounds were determined by FTIR, MS, 1H, 13C{1H} and 31P{1H} NMR spectral data. The solid-state structure of cis-5b was examined by single-crystal X-ray diffraction techniques. In addition, the compounds were tested in HeLa cancer cell lines using MTT assay … |
| Anahtar Kelimeler |
| Antimicrobial activity | Cytotoxicity | DNA interaction | Ferrocenylphosphazenes | Spectroscopy |
| Atıf Sayıları | |
| Web of Science | 47 |
| Scopus | 52 |
| Google Scholar | 61 |
| Dergi Adı | JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY |
| Yayıncı | Springer Science and Business Media Deutschland GmbH |
| Açık Erişim | Hayır |
| ISSN | 0949-8257 |
| E-ISSN | 1432-1327 |
| CiteScore | 5,2 |
| SJR | 0,513 |
| SNIP | 0,637 |