Effects of Steric Constraint on Chromium(III) Complexes of Tetraazamacrocycles, 2. Comparison of the Chemistry and Photobehavior of thetrans-Dichloro- andtrans-Dicyano- Complexes of Cyclam, 1,4-C2-Cyclam, and 1,11-C3-Cyclam†

2005 ◽  
Vol 44 (25) ◽  
pp. 9518-9526 ◽  
Author(s):  
Paul S. Wagenknecht ◽  
Chuanjiang Hu ◽  
Denise Ferguson ◽  
Lawrence C. Nathan ◽  
Robert D. Hancock ◽  
...  
Keyword(s):  
2007 ◽  
Vol 360 (5) ◽  
pp. 1482-1492 ◽  
Author(s):  
Michael T. Vagnini ◽  
W. Caleb Rutledge ◽  
Chuanjiang Hu ◽  
Donald G. VanDerveer ◽  
Paul S. Wagenknecht
Keyword(s):  

2011 ◽  
Vol 2011 ◽  
pp. 1-10 ◽  
Author(s):  
Matthew J. Crawford ◽  
Srinivas Rapireddy ◽  
Raman Bahal ◽  
Iulia Sacui ◽  
Danith H. Ly

Conformationally preorganized peptide nucleic acids (PNAs) have been synthesized through backbone modifications at the γ-position, where R = alanine, valine, isoleucine, and phenylalanine side chains. The effects of these side-chains on the conformations and hybridization properties of PNAs were determined using a combination of CD and UV-Vis spectroscopic techniques. Our results show that the γ-position can accommodate varying degrees of sterically hindered side-chains, reaffirming the bimodal function of PNAs as the true hybrids of “peptides” and “nucleic acids.”


2005 ◽  
Vol 127 (46) ◽  
pp. 16036-16037 ◽  
Author(s):  
Yuki Sudo ◽  
Yuji Furutani ◽  
Akimori Wada ◽  
Masayoshi Ito ◽  
Naoki Kamo ◽  
...  

1987 ◽  
Vol 52 (8) ◽  
pp. 1409-1413 ◽  
Author(s):  
Jun Nishimura ◽  
Akihiro Ohbayashi ◽  
Yuzuru Horiuchi ◽  
Yukihiro Okada ◽  
Shunichi Yamanaka ◽  
...  

1975 ◽  
Vol 53 (17) ◽  
pp. 2580-2585 ◽  
Author(s):  
J. H. Basso ◽  
S. Delattre ◽  
R. Lanteri ◽  
R. Luft

An examination of spectroscopic data for 43 alkenes reveals the influence of increasing substitution at the carbon atoms α or β to the ethylenic bond. The presence of a particularly large steric constraint requires that there be a single preferred molecular conformation: in such a case the frequency of the νC = C vibrator is strongly decreased (10 cm−1).A quantitative analysis of the phenomenon can be achieved using the "topological-chemical method D.A.R.C.". Topologic-information relationships could be developed for the two series 2-alkylethylenes and 2,2-dialkylethylenes. These permit the calculation of the contribution of each topological site to the frequency νC = C. For the first series, the relationship, based on 9 compounds, permits predictions about 30 others. For the second series, deductions are made concerning 159 compounds from a relationship established on a base of 13 compounds. [Journal translation]


1996 ◽  
Vol 37 (42) ◽  
pp. 7627-7630 ◽  
Author(s):  
Corrada Geraci ◽  
Mario Piattelli ◽  
Placido Neri

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