Department of Chemistry, University of Washington , Box 351700, Seattle, Washington 98195, United States.
Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey , New Brunswick, New Jersey 08903, United States.
Acc Chem Res. 2017 Mar 21;50(3):620-626. doi: 10.1021/acs.accounts.6b00621.
Great progress has been made in the past several decades concerning C-H bond functionalization. But despite many significant advances, a commercially viable large-scale process for selective alkane functionalization remains an unreached goal. Such conversions will require highly active, selective, and long-lived catalysts. In addition, essentially complete atom-economy will be required. Thus, any reagents used in transforming the alkanes must be almost free (e.g., O, HO, N), or they should be incorporated into the desired large-scale product. Any side-products should be completely benign or have value as fuels (e.g., H or other alkanes). Progress and promising leads toward the development of such systems involving primarily molecular transition metal catalysts are described.
在过去几十年中,C-H 键功能化取得了巨大进展。但尽管取得了许多重大进展,选择性烷烃功能化的商业可行大规模工艺仍然是一个尚未实现的目标。这种转化需要高活性、选择性和长寿命的催化剂。此外,还需要基本完全的原子经济性。因此,用于转化烷烃的任何试剂必须几乎是免费的(例如,O、HO、N),或者它们应该被整合到所需的大规模产品中。任何副产物都应该是完全良性的,或者具有作为燃料的价值(例如,H 或其他烷烃)。本文描述了在开发主要涉及分子过渡金属催化剂的此类系统方面的进展和有希望的线索。