62336-67-8Relevant articles and documents
Spatially controlled surface immobilization of nonmodified peptides
Pauloehrl, Thomas,Welle, Alexander,Bruns, Michael,Linkert, Katharina,B?rner, Hans G.,Bastmeyer, Martin,Delaittre, Guillaume,Barner-Kowollik, Christopher
, p. 9714 - 9718 (2013/09/23)
A phencyclone derivative is used to achieve light-controlled immobilization of peptides possessing only natural amino acids. The photoactive precursor (blue in picture) is formed in a Diels-Alder reaction and can undergo light-triggered ring-opening reactions with amines. Successful surface patterning with a genuine c(RGDfK) peptide (green) is evidenced by imaging time-of-flight secondary-ion mass spectrometry (ToF-SIMS). Copyright
A Study of Substituent Effects on Hydrogen-to-Arene Nonbonded Interactions
L'Esperance, Robert P.,Engen, Donna Van,Dayal, Rajeev,Pascal, Robert A.
, p. 688 - 694 (2007/10/02)
The polycyclic aromatic hydrocarbon 9,14-diphenylbenzotriphenylene is strongly twisted due to nonbonded interactions between hydrogen atoms on the polycyclic nucleus and the ? systems of the phenyl groups.Ten derivatives of 9,14-diphenylbenzotriphen