Syntheses and structural studies of mononuclear arene ruthenium complexes with nitrogen-based chelating ligands

2012 ◽  
Vol 65 (14) ◽  
pp. 2523-2534 ◽  
Author(s):  
Gajendra Gupta ◽  
Bruno Therrien ◽  
Sunhong Park ◽  
Shim Sung Lee ◽  
Jinkwon Kim
2007 ◽  
Vol 60 (20) ◽  
pp. 2177-2190 ◽  
Author(s):  
Nikhil Ranjan Pramanik ◽  
Saktiprosad Ghosh ◽  
Tapas Kumar Raychaudhuri ◽  
Siddhartha Chaudhuri ◽  
Mike G. B. Drew ◽  
...  

2018 ◽  
Vol 47 (44) ◽  
pp. 15772-15782 ◽  
Author(s):  
JuanJuan Li ◽  
Zhenzhen Tian ◽  
Zhishan Xu ◽  
Shumiao Zhang ◽  
Yaqian Feng ◽  
...  

A new class of half-sandwich Ir and Ru compounds containing P^P-chelating ligands can be developed as potential multifunctional theranostic platforms that combine bioimaging and anticancer capabilities.


2011 ◽  
Vol 637 (10) ◽  
pp. 1334-1340 ◽  
Author(s):  
Michael I. Bruce ◽  
Alexandre Burgun ◽  
Guillaume Grelaud ◽  
Martyn Jevric ◽  
Brian K. Nicholson ◽  
...  

2019 ◽  
Vol 195 ◽  
pp. 91-100 ◽  
Author(s):  
János P. Mészáros ◽  
Jelena M. Poljarevic ◽  
G. Tamás Gál ◽  
Nóra V. May ◽  
Gabriella Spengler ◽  
...  

2009 ◽  
Vol 48 (16) ◽  
pp. 2964-2968 ◽  
Author(s):  
Yann Gloaguen ◽  
Gilles Alcaraz ◽  
Anne-Frédérique Pécharman ◽  
Eric Clot ◽  
Laure Vendier ◽  
...  

2004 ◽  
Vol 357 (4) ◽  
pp. 1213-1218 ◽  
Author(s):  
Sylvain Burger ◽  
Bruno Therrien ◽  
Georg Süss-Fink

1988 ◽  
Vol 66 (3) ◽  
pp. 377-384 ◽  
Author(s):  
Wolfgang Kliegel ◽  
Steven J. Rettig ◽  
James Trotter

The preparation of the title compounds demonstrates the bis-N-alkylation of secondary amines by formaldehyde, these labile ammonium inner salts being captured as diphenylboron chelates. Crystals of 5,5-trimethylene-2,2-diphenyl-1,3-dioxa-5-azonia-2-boratacyclohexane are orthorhombic, a = 8.8461(3), b = 10.7290(4), c = 15.8773(5) Å, Z = 4, space group P212121, and those of 5,5-dimethyl-2,2-diphenyl-1,3-dioxa-5-azonia-2-boratacyclohexane monohydrate are monoclinic, a = 6.2432(3), b = 17.1469(8), c = 14.3701(5) Å, β = 90.647(3)°, Z = 4, space group P21/n. Both structures were solved by direct methods and were refined by full-matrix least-squares procedures to R = 0.030 and 0.047 for 1400 and 2258 reflections with I ≥ 3σ(I), respectively. Both compounds have a B,N-betaine structure, the six-membered chelate rings adopting chair conformations. Libration-corrected bond lengths, O—B = 1.508(3)−1.522(3) and C—B = 1.612(4)−1.637(4) Å, indicate relatively strong binding of the diphenylboron moiety to the oxygen atoms of the O,O-chelating ligands.


2004 ◽  
Vol 689 (4) ◽  
pp. 879-882 ◽  
Author(s):  
Manoj Trivedi ◽  
Manish Chandra ◽  
Daya Shankar Pandey ◽  
M.Carmen Puerta ◽  
Pedro Valerga

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