Duplex strand formation using alternating copolymers was written by Nakade, Hiroshi;Ilker, M. Firat;Jordan, Brian J.;Uzun, Oktay;LaPointe, Nicholas L.;Coughlin, E. Bryan;Rotello, Vincent M.. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2005.Recommanded Product: N-(6-Aminopyridin-2-yl)acetamide This article mentions the following:
The regular arrangement of complementary diaminopyridine-thymine (DAP-THY) on alternating diaminopyridine-thymine functionalized 7-oxanorbornene-cyclooctene copolymers permits cooperative binding events and the effective formation of well-controlled micrometer-scale aggregates. The formation of duplex supramol.-copolymer complex relative to stoichiometry and the binding affinity between complementary functionalized alternating copolymers was determined The alternating copolymers were prepared using ring opening metathesis polymerization (ROMP) giving between 92 and 98% alternating units. In the experiment, the researchers used many compounds, for example, N-(6-Aminopyridin-2-yl)acetamide (cas: 1075-62-3Recommanded Product: N-(6-Aminopyridin-2-yl)acetamide).
N-(6-Aminopyridin-2-yl)acetamide (cas: 1075-62-3) belongs to pyridine derivatives. The ring atoms in the pyridine molecule are sp2-hybridized. The nitrogen is involved in the π-bonding aromatic system using its unhybridized p orbital. The lone pair is in an sp2 orbital, projecting outward from the ring in the same plane as the σ bonds. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Recommanded Product: N-(6-Aminopyridin-2-yl)acetamide