Keyword search (4,163 papers available)

"Cuccia LA" Authored Publications:

Title Authors PubMed ID
1 Improving diacetylene photopolymerization in monolayers and ultrathin films Ji J; Li Y; Bernaerts S; Mali KS; Ding R; Lin H; Cuccia LA; De Feyter S; Ivasenko O; Chi L; Fang Y; 40171944
CHEMBIOCHEM
2 Revisiting Homochiral versus Heterochiral Interactions through a Long Detective Story of a Useful Azobis-Nitrile and Puzzling Racemate García de la Concepción J; Flores-Jiménez M; Cuccia LA; Light ME; Viedma C; Cintas P; 37547876
CHEMBIOCHEM
3 On the Origin of Sugar Handedness: Facts, Hypotheses and Missing Links-A Review Martínez RF; Cuccia LA; Viedma C; Cintas P; 35796896
CHEMBIOCHEM
4 Electrospun Upconverting Nanofibrous Hybrids with Smart NIR-Light-Controlled Drug Release for Wound Dressing Huang HY; Skripka A; Zaroubi L; Findlay BL; Vetrone F; Skinner C; Oh JK; Cuccia LA; 35019380
CHEMBIOCHEM
5 Pasteur made simple - mechanochemical transformation of racemic amino acid crystals into racemic conglomerate crystals. Viedma C, Lennox C, Cuccia LA, Cintas P, Ortiz JE 32202285
NA
6 Oriented attachment by enantioselective facet recognition in millimeter-sized gypsum crystals. Viedma C, Cuccia LA, McTaggart A, Kahr B, Martin AT, McBride JM, Cintas P 27722508
CHEMBIOCHEM
7 Directing the Viedma ripening of ethylenediammonium sulfate using "Tailor-made" chiral additives. Nguyen TP, Cheung PS, Werber L, Gagnon J, Sivakumar R, Lennox C, Sossin A, Mastai Y, Cuccia LA 27722259
CHEMBIOCHEM
8 Alkyl chain length effects on double-deck assembly at a liquid/solid interface. Fang Y, Cibian M, Hanan GS, Perepichka DF, De Feyter S, Cuccia LA, Ivasenko O 30052249
CHEMBIOCHEM
9 Structural organization and phase behaviour of meta-substituted dioctadecylaminobenzoquinones at the air/water interface. Behyan S, Gritzalis D, Schmidt R, Kebede E, Cuccia LA, DeWolf C 30657501
CNSR

 

Title:Directing the Viedma ripening of ethylenediammonium sulfate using "Tailor-made" chiral additives.
Authors:Nguyen TP,  Cheung PS,  Werber L,  Gagnon J,  Sivakumar R,  Lennox C,  Sossin A,  Mastai Y,  Cuccia LA
Link:https://www.ncbi.nlm.nih.gov/pubmed/27722259?dopt=Abstract
Publication:
Keywords:
PMID:27722259 Category:Chem Commun (Camb) Date Added:2019-05-31
Dept Affiliation: CHEMBIOCHEM
1 Department of Chemistry & Biochemistry, Concordia University, 7141 Sherbrooke Street West, Montréal, Québec H4B 1R6, Canada. Louis.Cuccia@concordia.ca.
2 Bar-Ilan University, Department of Chemistry, Ramat Gan, Israel. Yitzhak.Mastai@biu.ac.il.

Description:

Directing the Viedma ripening of ethylenediammonium sulfate using "Tailor-made" chiral additives.

Chem Commun (Camb). 2016 Oct 18;52(85):12626-12629

Authors: Nguyen TP, Cheung PS, Werber L, Gagnon J, Sivakumar R, Lennox C, Sossin A, Mastai Y, Cuccia LA

Abstract

Both enantiomers of trans-cyclohexane-1,2-diammonium sulfate and trans-1,2-diphenylethylenediammonium sulfate were used as "tailor-made" additives to direct the mirror-symmetry breaking in the attrition-enhanced deracemization (i.e. Viedma ripening) of conglomerate crystals of ethylenediammonium sulfate (EDS). Isothermal titration calorimetry (ITC) shows chiral recognition of (1R,2R)- and (1S,2S)-1,2-diphenylethylenediamine to EDS crystals where the enthalpy of adsorption of the (1R,2R)-isomer on l-EDS crystals is higher in comparison to that on d-EDS crystals. These results are consistent with a "rule of reversal" mechanism driving the chiral outcome of the Viedma ripening of EDS.

PMID: 27722259 [PubMed]




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