A chiral porous organic cage for molecular recognition using gas chromatography.
Kunming, China. In Anal Chim Acta, Feb 2016
By comparing the chiral recognition ability of the CC9-coated column with the commercially available β-DEX 120 column and the POC CC3-R coated column recently reported by our group, the CC9-coated column offered good resolution during the separation of some racemates, that were not separated using the β-DEX 120 column or POC CC3-R coated column.
Porous organic cages for sulfur hexafluoride separation.
In J Am Chem Soc, Feb 2016
Despite lacking any metal sites, a porous cage, CC3, shows the highest SF6/N2 selectivity reported for any material at ambient temperature and pressure, which translates to real separations in a gas breakthrough column.
Highly selective separation of enantiomers using a chiral porous organic cage.
Shanghai, China. In J Chromatogr A, Jan 2016
The fabricated column complements to commercial β-DEX 120 column and our recently reported CC3-R column for separating enantiomers, which indicates that the excellent chiral recognition ability of CC10 is not only interesting academically, but also has potential for practical application.
Morphokinetics of embryos developed from oocytes matured in vitro.
Monza, Italy. In J Assist Reprod Genet, Jan 2016
The morphokinetics of embryos selected for transfer or cryopreservation, derived from EC-MII and CC oocytes, were comparatively and retrospectively analyzed in terms of cleavage times (t2, t3, t4, t5, and t8) and intervals (cc2, cc3, s2, s3).
ITSN2L Interacts with and Negatively Regulates RABEP1.
Changsha, China. In Int J Mol Sci, 2014
In this study, RABEP1 was identified as a novel ITSN2L interacting protein using a yeast two-hybrid screen from a human brain cDNA library and this interaction, specifically involving the ITSN2L CC domain and RABEP1 CC3 regions, was further confirmed by in vitro GST (glutathione-S-transferase) pull-down and in vivo co-immunoprecipitation assays.
Parallel Calculation of CCSDT and Mk-MRCCSDT Energies.
Mainz, Germany. In J Chem Theory Comput, 2010
A scheme for the parallel calculation of energies at the coupled-cluster singles, doubles, and triples (CCSDT) level of theory, several approximate iterative CCSDT schemes (CCSDT-1a, CCSDT-1b, CCSDT-2, CCSDT-3, and CC3), and for the state-specific multireference coupled-cluster ansatz suggested by Mukherjee with a full treatment of triple excitations (Mk-MRCCSDT) is presented.