Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Brent E. Dial"'
Autor:
Xiaomin Tang, Changhao Liu, Jong Keum, Jihua Chen, Brent E. Dial, Yangyang Wang, Wan-Yu Tsai, Wim Bras, Tomonori Saito, Christopher C. Bowland, X. Chelsea Chen
Publikováno v:
RSC Advances. 12:10886-10894
With the continuous increase of global plastics production, there is a demand to develop energy efficient processes to transform mixed plastic wastes into new products with enhanced utility - a concept that is often referred to as upcycling. Compatib
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Publikováno v:
Chemical Science. 6:4358-4364
In this study, the contributions of London dispersion forces to the strength of aromatic stacking interactions in solution were experimentally assessed using a small molecule model system. A series of molecular torsion balances were designed to measu
Autor:
Erik C. Vik, Amanda E. Rickher, Christopher J. Yehl, Mark D. Smith, Ken D. Shimizu, Ping Li, Josef M. Maier, Perry J. Pellechia, Brent E. Dial
Publikováno v:
Angewandte Chemie (International ed. in English). 56(25)
A series of N-arylimide molecular balances were designed to study and measure fluorine–aromatic (F–π) interactions. Fluorine substituents gave rise to increasingly more stabilizing interactions with more electron-deficient aromatic surfaces. The
Autor:
Ken D. Shimizu, Roger D. Rasberry, Brent E. Dial, Perry J. Pellechia, Salvatore Profeta, Mark D. Smith, Brooke N. Bullock
Publikováno v:
Organic Letters. 13:244-247
A molecular rotor was designed in which the rate of rotation is accelerated by guest complexation. The binding of an acetate guest to the urea groups lowers the barrier of the adjacent C(aryl)-N(imide) bond by 2 to 4 kcal/mol. This behavior is in con
Publikováno v:
Journal of the American Chemical Society. 134(8)
A molecular rotor was designed that rotates 7 orders of magnitude faster upon protonation. The quinoline rotor is based on a rigid N-arylimide framework that displays restricted rotation due to steric interaction between the quinoline nitrogen and im
Publikováno v:
Chemical communications (Cambridge, England). 48(9)
Demonstrated is the reversible switching and saving of a conformational molecular switch via heating in different environments followed by reversible chemical entrapment.
Autor:
Brent E. Dial, Roger D. Rasberry, Brooke N. Bullock, Mark D. Smith, Perry J. Pellechia, Salvatore Profeta, Ken D. Shimizu
Publikováno v:
Organic Letters; Jan2011, Vol. 13 Issue 2, p244-247, 4p