scholarly journals Enabling online determination of the size-dependent RNA content of lipid nanoparticle-based RNA formulations

2021 ◽  
pp. 123015
Author(s):  
Xiujuan Jia ◽  
Yong Liu Conceptulization ◽  
Angela M. Wagner ◽  
Michelle Chen ◽  
Yuejie Zhao ◽  
...  
1989 ◽  
Vol 4 (4) ◽  
pp. 239-251 ◽  
Author(s):  
Yaxia Xie ◽  
Thomas Herget ◽  
Joachim Hallmayer ◽  
Anna Starzinski-Powitz ◽  
Konstantin -Alexander Hossmann
Keyword(s):  

1991 ◽  
Vol 5 (1) ◽  
pp. 39-42 ◽  
Author(s):  
S. Benthin ◽  
J. Nielsen ◽  
J. Villadsen
Keyword(s):  

1994 ◽  
Vol 349 ◽  
Author(s):  
Andrew A. Quong ◽  
Mark R. Pederson

ABSTRACTWe use the local-density-approximation to the density-functional theory to determine the axial polarizabilities of fullerene tubules as a function of length and winding topologies. Specifically, we present linear polarizabilities for tubules of composition C12H24, C36H24, C40H20 and C60H24. The size-dependent variation in the dipole-coupled gaps between pairs of occupied and unoccupied levels leads to enhancements in the polarizability per valence electron as the length of the tubule increases. The results are compared to recent densityfunctional based calculations of the linear and nonlinear polarizabilities for fullerene and benzene molecules.


1998 ◽  
Vol 32 (11) ◽  
pp. 1615-1622 ◽  
Author(s):  
Peter F. Caffrey ◽  
John M. Ondov ◽  
Maria J. Zufall ◽  
Cliff I. Davidson

1991 ◽  
Vol 8 (1-4) ◽  
pp. 315-322 ◽  
Author(s):  
Yu-Chen Chang ◽  
Richard V. Calabrese ◽  
James W. Gentry
Keyword(s):  

2021 ◽  
Author(s):  
Zetan Cao ◽  
Jia He ◽  
Zhiwen Liu ◽  
Haoran Zhang ◽  
Bin Chen

Abstract Chirality involved reactions enable to probe features in the fields of asymmetric synthesis and catalysis, which allow to gain insight into the fundamental mechanisms of topochemically controlled reactions. However, in situ observation of the chirality-associated reaction dynamics with simultaneous structural determination of new features has been lacking. Here, we report the direct visualization of the electron-beam-stimulated reaction dynamics of HgS nanostructures with chiral and achiral morphologies simultaneously in both real and reciprocal space. Under the electron-beam excitation of HgS nanostructures, the formation and evaporation dynamics of Hg nanodroplets were vividly pictured while the reciprocal space imaging revealed the structural transformation from monocrystalline to polycrystalline. Such induced changes were size-dependent, which were slowed down when involving the chirality in the nanostructures. The finding offers a fundamental understanding of topochemically controlled reaction mechanisms and holds promise of tuning asymmetric synthesis for catalysis related applications.


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