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По вашему запросу найдено документов: 23

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Exploring mechanisms in Ni terpyridine catalyzed C-C cross-coupling reactions-A review
,2':6',2''-terpyridine (tpy) stands as an excellent example of these ligands. This review summarizes research that has
Thiacalix[4]monocrowns with terpyridine functional groups as new structural units for luminescent polynuclear lanthanide complexes
Muravev A., Galieva F., Bazanova O., Sharafutdinova D., Solovieva S., Antipin I., Konovalov A.
Thiacalix[4]monocrowns with terpyridine functional groups as new structural units for luminescent
New iridium bis‐terpyridine complexes: synthesis, characterization, antibiofilm and anticancer potentials
Sahin C., Mutlu D., Nasirli F., Mahmoudi G., Zubkov F.I., Arslan S., Dogan N.M.
, and cytotoxicity of iridium bis-terpyridine complexes. The complexes were characterized by NMR, MS, FTIR, UV
Thiacalix[4]monocrowns with terpyridine functional groups as new structural units for luminescent polynuclear lanthanide complexes
Muravev A., Galieva F., Bazanova O., Sharafutdinova D., Solovieva S., Antipin I., Konovalov A.
Thiacalix[4]monocrowns with terpyridine functional groups as new structural units for luminescent
New terpyridine derivatives of thiacalix[4]arenes in solution and at the water-air interface
Muravev A.A., Agarkov A.S., Galieva F.B., Yakupov A.T., Bazanova O.B., Rizvanov I.K., Shokurov A.V., Zaitseva A.V., Selektor S.L., Solovieva S.E., Antipin I.S.
in cone and 1,3-alternate configurations containing terpyridine and triazole fragments at the lower rim
A New Concept of Enhancing the Anticancer Activity of Manganese Terpyridine Complex by Oxygen-Containing Substituent Modification
Li J., Chen M., Jiang J., Huang J., Chen H., Pan L., Nesterov D.S., Ma Z., Pombeiro A.J.L.
Eleven manganese 4′-substituted-2,2′:6′,2″-terpyridine complexes (1a–1c and 2a–2h) with three non
Synthesis and fluorescent properties of thiacalix[4]arenes containing terpyridyl fragments at the lower rim
Muravev A., Burilov V., Solov'eva S., Strel'nik A., Latypov S., Bazanova O., Sharafutdinova D., Antipin I., Konovalov A.
Terpyridines
Terpyridine isomerism as a tool for tuning red-to-NIR emissive properties in heteronuclear gold(i)–thallium(i) complexes
Royo David, Moreno Sonia, Rodríguez-Castillo María, Monge Miguel, Olmos M.E., Zubkov F.I., Pronina A.A., Mahmoudi Ghodrat, López-de-Luzuriaga J.M.
Terpyridine ligand isomerism permits the tuning of the emissions in heteropolynuclear gold
Synthesis and fluorescent properties of thiacalix[4]arenes containing terpyridyl fragments at the lower rim
Muravev A., Burilov V., Solov'eva S., Strel'nik A., Latypov S., Bazanova O., Sharafutdinova D., Antipin I., Konovalov A.
Terpyridines
2D and 3D Zn(II) coordination polymers based on 4′-(Thiophen-2-yl)-4,2′:6′,4′'-terpyridine: Structures and features of sorption behavior
Zaguzin A.S., Mahmoudi G., Sukhikh T.S., Sakhapov I.F., Zherebtsov D.A., Zubkov F.I., Valchuk K.S., Sokolov M.N., Fedin V.P., Adonin S.A.
Reactions of Zn(II) nitrate, 4′-(Thiophen-2-yl)-4,2′:6′,4′'-terpyridine (ThioTerPy) and terephtalic

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