We describe a bottom-up surface functionalization to design hybrid molecular coatings that tether biomembranes using wet chemistry. First, a monolayer was formed by immersion in a NH-Ar-SOH solution, allowing aryldiazonium salt radicals to spontaneously bind to it via strong C bonding. After formation of the air-stable and dense molecular monolayer (-Ar-SOH), a subsequent activation was used to form highly reactive -Ar-SOCl groups nearly perpendicular to the monolayer.
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