Cyanoisocyanoarene Metal Complexes as Building Blocks for Coordination Polymers:  Structural Nonrigidity of a Metal−Nitrile Linkage1

1998 ◽  
Vol 37 (22) ◽  
pp. 5776-5780 ◽  
Author(s):  
Andreas Mayr ◽  
Li-Feng Mao
2009 ◽  
Vol 131 (15) ◽  
pp. 5393-5395 ◽  
Author(s):  
Tomasz Kaczorowski ◽  
Iwona Justyniak ◽  
Teodozja Lipińska ◽  
Janusz Lipkowski ◽  
Janusz Lewiński

Author(s):  
Tong Cao ◽  
Francisco Javier Valverde-Muñoz ◽  
Xiaoyi Duan ◽  
Mingjian Zhang ◽  
Ping Wang ◽  
...  

2001 ◽  
Vol 121 (1-3) ◽  
pp. 1249-1252 ◽  
Author(s):  
U.S. Schubert ◽  
C. Eschbaumer ◽  
P. Andres ◽  
H. Hofmeier ◽  
C.H. Weidl ◽  
...  

2017 ◽  
Vol 53 (35) ◽  
pp. 4748-4758 ◽  
Author(s):  
Balaram Mohapatra ◽  
Pratibha Pratibha ◽  
Sandeep Verma

This feature article outlines design strategies for modified adenine derivatives to construct discrete metal complexes, ring-expanded skeletons, coordination polymers, MOFs, and capped nanoparticles, for applications in gas adsorption, as bioimaging agents and as bioactive molecules.


2009 ◽  
Vol 38 (6) ◽  
pp. 1690 ◽  
Author(s):  
Gianluca Accorsi ◽  
Andrea Listorti ◽  
K. Yoosaf ◽  
Nicola Armaroli

2014 ◽  
Vol 18 (01n02) ◽  
pp. 115-122 ◽  
Author(s):  
Srinivas Banala ◽  
Klaus Wurst ◽  
Bernhard Kräutler

We report here the preparation (in "one-pot") of a tetra-β″-sulfoleno-meso-aryl-porphyrin in about 80% yield by using an optimized modification of Lindsey's variant of the Adler–Longo approach. The Zn ( II )-, Cu ( II )- and Ni ( II )-complexes of the symmetrical porphyrin were prepared and characterized spectroscopically. Crystal structures of the fluorescent Zn ( II )- and of the non-fluorescent Ni ( II )-tetra-β″-sulfoleno-meso-aryl-porphyrinates showed the highly substituted porphyrin ligands to be nearly perfectly planar. The Zn ( II )-complex of this porphyrin has been used as a thermal precursor of a reactive diene, and — formally — of lateral and diagonal bis-dienes, of a tris-diene and of a tetra-diene, which all underwent [4 + 2]-cycloaddition reactions in situ with a range of dienophiles. Thus, the tetra-β″-sulfoleno-meso-aryl-porphyrin and its metal complexes represent reactive building blocks, "programmed" for the syntheses of symmetrical and highly functionalized porphyrins.


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