Abstract
A cellulose paper sheet, chemically modified with azide functions, is described to be a versatile molecular platform for copper-catalyzed 1,3-dipolar cycloaddition with terminal alkynes. This 3-step methodology was carefully optimized at each stage of the process with the support of experimental and physical evidences. Our approach allows the surface coverage of structurally diverse molecular architectures through a covalent grafting with non-hydrolysable chemical linkers. This robust linkage is highlighted with the surface hydrophobization of cellulose paper through the click ligation of cholesterol units as renewable and inexpensive hydrophobic agents. The resulting water-resistant and water-repellent paper-based material shows powerful oleophilicity properties and displays a high contact angle of 139.6°.