In the original paper Phys. Rev. D 95, 052004 (2017), "Measurements of charm mixing and CP violation using D 0 → K AE π ∓ decays," the systematic uncertainties reported in Table II regarding the doubly tagged (DT) only result for ðx 0þ Þ 2 and y 0þ were swapped in both the "no direct CPV" and "all CPV allowed" fits. All other reported values are correct. The corrected table is shown below in Table II.
Control over hydrogen bonding patterns and the dimensionality of supramolecular structures is possible through covalent assisted supramolecular synthesis. Consistent and predictable 'masking' of the amide functionality has been achieved through the covalent modification of isoniazid with benzophenone and benzophenone derivatives while co-crystallizing with salicylic acid. A series of co-crystals using benzophenones as masking agents was prepared using one-pot synthetic methods. No short intermolecular contacts were present between the amide nitrogen atoms in isoniazid and neighbouring isoniazid or salicylic acid atoms.
Eight
co-crystals of covalently modified isoniazid were synthesized,
using either 3- or 4-hydroxybenzoic acid as the co-former. It was
demonstrated that, for the co-crystallization of “masked”
isoniazid by benzophenone derivatives, a small change in reaction
or crystallization conditions played a large role in the outcome of
the resulting supramolecular structure, whereas the addition of either
one or two methyl substituents to the benzophenone rings did not affect
the supramolecular structure of the resulting co-crystals. Changing
the reflux time for the supramolecular synthesis resulted in stoichiometric
variation. Adding larger quantities of one of the starting supramolecular
reagents as “additives” resulted in polymorphism. Using
a catalyst for the covalent modification of isoniazid during one-pot
supramolecular synthesis prevented the formation of a solvate.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.