62336-67-8Relevant academic research and scientific papers
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
supporting information, 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
Tuning the singlet-triplet gap in metal-free phosphorescent π-conjugated polymers
Chaudhuri, Debangshu,Wettach, Henning,Van Schooten, Kipp J.,Liu, Su,Sigmund, Eva,Hoeger, Sigurd,Lupton, John M.
supporting information; experimental part, p. 7714 - 7717 (2010/12/25)
Glow in the dark: A tunable singlet-triplet exchange gap arises in optically active conjugated polymers that exhibit both strong fluorescence from the singlet state and pronounced phosphorescence from triplet excitations (see picture). The polymers were incorporated into organic light-emitting diodes (OLEDs).
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
