Nanocellulose, typically cellulose nanocrystals (CNCs), has excellent properties and is widely used. In particular, CNC has a small dimension, high chemical reactivity, and high sustainability, which makes it an excellent candidate as a starting material to be converted into nanocellulose derivatives. Chemical modification is essential for obtaining the desired products; the modifications create different functional attachment levels and generate novel microstructures. Recent advances on nanocellulose derivatives have not yet been reviewed and evaluated for the last five years. Nanocellulose derivative materials are being used in a wide variety of high-quality functional applications. To meet these requirements, it is essential for researchers to fully understand CNCs and derivative materials, precisely their characteristics, synthesis methods, and chemical modification approaches. This paper discusses CNC and its derivatives concerning the structural characteristics, performance, and synthesis methods, comparing the pros and cons of these chemical modification approaches reported in recent years. This review also discusses the critical physicochemical properties of CNC derivative products, including solubility, wetting performance, and associated impacts on properties. Lastly, this paper also comments on the bottlenecks of nanocellulose derivatives in various applications and briefly discusses their future research direction.

Cellulose nanocrystal (CNC) is a nanoscale colloid with superior potential for coatings, liquid crystal displays, and optoelectronics. However, to date, the presence of hydrophilicity still limits its application. Multifunction via graft copolymerization modification of CNC appears to be breaking into a new direction. In this study, we used the residual hydroxyl groups on the CNC to react with 2-bromoisobu-tyryl bromide, and the initiator was therefore anchored on the CNC surface. Through atom transfer radical polymerization (ATRP), CNC was successfully grafted to azobenzene monomer, i.e., 9-[4-[2-[4-(trifluorometh) phenyl] diazenyl] phenoxy] nonayl acrylate (FAZO). After a series of characterization methods, such as FTIR, NMR and XRD, it was found that the surface water contact angle of the CNC-PFAZO prepared by the modification was as high as 134.4°, and the high hydrophilicity of this material could be maintained for up to one month, even longer.