Redox-active, near-infrared dyes based on ‘Nindigo’ (indigo-N,N′-diarylimine) boron chelate complexes

2013 ◽  
Vol 4 (2) ◽  
pp. 612-621 ◽  
Author(s):  
Graeme Nawn ◽  
Simon R. Oakley ◽  
Marek B. Majewski ◽  
Robert McDonald ◽  
Brian O. Patrick ◽  
...  
Author(s):  
Rui-Zhe Zhang ◽  
Xiao Feng ◽  
Ying Liu ◽  
Sheng-Qing Wang ◽  
Jin-Ting Liu ◽  
...  

1989 ◽  
Vol 200 ◽  
pp. 61-72 ◽  
Author(s):  
M.S. Korobov ◽  
G.S. Borodkin ◽  
N.I. Borisenko ◽  
T.A. Ryskina ◽  
L.E. Nivorozhkin ◽  
...  

ChemInform ◽  
1990 ◽  
Vol 21 (7) ◽  
Author(s):  
M. S. KOROBOV ◽  
G. S. BORODKIN ◽  
N. I. BORISENKO ◽  
T. A. RYSKINA ◽  
L. E. NIVOROZHKIN ◽  
...  

2016 ◽  
Vol 52 (36) ◽  
pp. 6103-6106 ◽  
Author(s):  
Daniel Fink ◽  
Bernhard Weibert ◽  
Rainer F. Winter

Tetraruthenium macrocycles with 1,4-divinylphenylene and diarylamine-substituted isophthalic acids as the sides display up to eight one-electron redox steps and rich electrochromic behaviour with strong absorptions of the dications in the near infrared and of the tetra- and hexacations at low energies in the visible.


2015 ◽  
Vol 112 (36) ◽  
pp. 11161-11168 ◽  
Author(s):  
Paul R. McGonigal ◽  
Pravas Deria ◽  
Idan Hod ◽  
Peyman Z. Moghadam ◽  
Alyssa-Jennifer Avestro ◽  
...  

The organization of trisradical rotaxanes within the channels of a Zr6-based metal–organic framework (NU-1000) has been achieved postsynthetically by solvent-assisted ligand incorporation. Robust ZrIV–carboxylate bonds are forged between the Zr clusters of NU-1000 and carboxylic acid groups of rotaxane precursors (semirotaxanes) as part of this building block replacement strategy. Ultraviolet–visible–near-infrared (UV-Vis-NIR), electron paramagnetic resonance (EPR), and 1H nuclear magnetic resonance (NMR) spectroscopies all confirm the capture of redox-active rotaxanes within the mesoscale hexagonal channels of NU-1000. Cyclic voltammetry measurements performed on electroactive thin films of the resulting material indicate that redox-active viologen subunits located on the rotaxane components can be accessed electrochemically in the solid state. In contradistinction to previous methods, this strategy for the incorporation of mechanically interlocked molecules within porous materials circumvents the need for de novo synthesis of a metal–organic framework, making it a particularly convenient approach for the design and creation of solid-state molecular switches and machines. The results presented here provide proof-of-concept for the application of postsynthetic transformations in the integration of dynamic molecular machines with robust porous frameworks.


1995 ◽  
Vol 32 (6) ◽  
pp. 213 ◽  
Author(s):  
Suresh Das ◽  
K. George Thomas ◽  
K. J. Thomas ◽  
M. V. George ◽  
I. Bedja ◽  
...  

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