Archives for Chemistry Experiments of 6602-54-6

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A catalyst don’t appear in the overall stoichiometry of the reaction it catalyzes, but it must appear in at least one of the elementary reactions in the mechanism for the catalyzed reaction. 6602-54-6, Name is 2-Chloronicotinonitrile, molecular formula is C6H3ClN2. In an article, author is Choi, Heekyoung,once mentioned of 6602-54-6, Category: pyridine-derivatives.

Dual Trapping of a Metastable Planarized Triarylborane pi-System Based on Folding and Lewis Acid-Base Complexation for Seeded Polymerization

We report the kinetically controlled supramolecular polymerization of boron-containing p-conjugated molecules, which was enabled by a seeding method based on dual trapping of a metastable state by synergistic intramolecular hydrogen bonding and Lewis acid-based complexation. Planarized triarylborane-based 1, which bears a diamide chain with chiral alkyl groups, was synthesized. Upon cooling, the solution of monomer 1 afforded a supramolecular polymerization in a cooperative manner to form helical supramolecular nanostructures with intense J-type aggregate emission. In the presence of pyridine, the triarylborane moiety formed a Lewis acid-base complex, which enhances the stabilization of the metastable monomeric state. An assembly incompetent structure with a folded diamide chain conformation and a pyridine moiety axially coordinated to the boron atom is responsible for slowing the spontaneous aggregation. The seeding method was successfully applied to the solution to produce homogeneous nanofibers even at a high (millimolar-level) concentration. This unprecedented kinetic control via dual trapping provides an effective method to achieve seed-initiated polymerization under concentrated conditions.

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Reference:
Pyridine – Wikipedia,
,Pyridine | C5H5N – PubChem