Perpendicularly Arranged Ruthenium Porphyrin Dimers and Trimers

1997 ◽  
Vol 36 (8) ◽  
pp. 1625-1635 ◽  
Author(s):  
Kenji Funatsu ◽  
Akira Kimura ◽  
Taira Imamura ◽  
Akio Ichimura ◽  
Yoichi Sasaki
1975 ◽  
Vol 97 (2) ◽  
pp. 277-281 ◽  
Author(s):  
Frederick R. Hopf ◽  
Terrence P. O'Brien ◽  
W. Robert Scheidt ◽  
David G. Whitten

1984 ◽  
Vol 106 (12) ◽  
pp. 3500-3510 ◽  
Author(s):  
James P. Collman ◽  
Craig E. Barnes ◽  
Paul N. Swepston ◽  
James A. Ibers

1989 ◽  
Vol 111 (20) ◽  
pp. 7806-7811 ◽  
Author(s):  
C. Drew Tait ◽  
James M. Garner ◽  
James P. Collman ◽  
Alfred P. Sattelberger ◽  
William H. Woodruff

2006 ◽  
Vol 32 (9) ◽  
pp. 677-693 ◽  
Author(s):  
S. Pheasant ◽  
J. A. Kouzelos ◽  
H. Van Ryswyk ◽  
R. J. Cave

1985 ◽  
Vol 107 (15) ◽  
pp. 4570-4571 ◽  
Author(s):  
James P. Collman ◽  
P. J. Brothers ◽  
L. McElwee-White ◽  
E. Rose ◽  
L. J. Wright

2000 ◽  
Vol 72 (12) ◽  
pp. 2265-2274 ◽  
Author(s):  
Jeremy K. M. Sanders

Two different approaches are described for the creation of supramolecular systems potentially capable of recognition and catalysis. Using the design approach, we have been able to accelerate and influence two different Diels­Alder reactions within the cavities of porphyrin dimers and trimers; this is templating from the outside inwards. The selection approach is a synthetic chemical attempt to capture some of the key evolutionary features of biological systems: dynamic combinatorial chemistry is used to create equilibrating mixtures of potential receptors, and then a template is used to select and amplify the desired system. Five potential reactions for such dynamic chemistry are discussed: base-catalyzed transesterification, hydrazone exchange, disulfide exchange, alkene metathesis, and Pd-catalyzed allyl exchange, and preliminary templating results (inside outwards) are presented.


Sign in / Sign up

Export Citation Format

Share Document