(1,2,3,4,7-Pentamethylindenyl)rhodium complexes with arene ligands

2007 ◽  
Vol 692 (26) ◽  
pp. 5777-5787 ◽  
Author(s):  
Dmitry A. Loginov ◽  
Mikhail M. Vinogradov ◽  
Zoya A. Starikova ◽  
Elena A. Petrovskaya ◽  
Piero Zanello ◽  
...  
2018 ◽  
Vol 37 (15) ◽  
pp. 2553-2562 ◽  
Author(s):  
Vladimir B. Kharitonov ◽  
Maria Makarova ◽  
Mikhail A. Arsenov ◽  
Yulia V. Nelyubina ◽  
Olga Chusova ◽  
...  

2006 ◽  
Vol 71 (2) ◽  
pp. 197-206 ◽  
Author(s):  
Martin Pošta ◽  
Jan Čermák ◽  
Pavel Vojtíšek ◽  
Ivana Císařová

The first rhodium complexes of diphosphinoazines [{RhCl(1,2-η:5,6-η-CH=CHCH2CH2CH=CHCH2CH2)}2 {μ-R2PCH2C(But)=NN=C(But)CH2PR2] (R = Ph, Cy, Pri) were prepared by cleavage of the bridge in chloro(cycloocta-1,5-diene)rhodium(I) dimer, the analogous iridium(I) complexes were also prepared for the first time. The X-ray structures of isostructural rhodium and iridium complexes with bis(dicyclohexylphosphino)pinacoloneazine were determined. Diphosphinoazine ligands in the complexes remained in (Z,Z) configuration bridging two RhCl(C8H12) units.


RSC Advances ◽  
2019 ◽  
Vol 9 (50) ◽  
pp. 29396-29404 ◽  
Author(s):  
Magdalena Jankowska-Wajda ◽  
Olga Bartlewicz ◽  
Andrea Szpecht ◽  
Adrian Zajac ◽  
Marcin Smiglak ◽  
...  

Platinum and rhodium complexes ligated by imidazolium substituted phosphine were obtained with high yields and applied as efficient catalysts.


Author(s):  
Gianpiero Cera ◽  
Andrea Secchi ◽  
Arturo Arduini ◽  
Gabriele Giovanardi

Molecules ◽  
2021 ◽  
Vol 26 (5) ◽  
pp. 1214
Author(s):  
Sergey N. Podyachev ◽  
Rustem R. Zairov ◽  
Asiya R. Mustafina

The present review is aimed at highlighting outlooks for cyclophanic 1,3-diketones as a new type of versatile ligands and building blocks of the nanomaterial for sensing and bioimaging. Thus, the main synthetic routes for achieving the structural diversity of cyclophanic 1,3-diketones are discussed. The structural diversity is demonstrated by variation of both cyclophanic backbones (calix[4]arene, calix[4]resorcinarene and thiacalix[4]arene) and embedding of different substituents onto lower or upper macrocyclic rims. The structural features of the cyclophanic 1,3-diketones are correlated with their ability to form lanthanide complexes exhibiting both lanthanide-centered luminescence and magnetic relaxivity parameters convenient for contrast effect in magnetic resonance imaging (MRI). The revealed structure–property relationships and the applicability of facile one-pot transformation of the complexes to hydrophilic nanoparticles demonstrates the advantages of 1,3-diketone calix[4]arene ligands and their complexes in developing of nanomaterials for sensing and bioimaging.


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