and alkyne (also called A 3 coupling) is a representative type of CH bond activation reaction to produce propargylamine and its derivatives, serving as an important intermediate for the synthesis of many nitrogen-containing biological and pharmaceutical compounds, which can be catalyzed by Au 0 and Au δ+ (δ > 0, representing the oxidation state of Au species) according to the previous reports. [8][9][10][11][12] For example, Liu et al. sythesized an Au/MIL-53(Al) catalyst-containing Au 0 and Au 3+ species, which display good activity for the A 3 coupling reaction. [13] In addition, Liu et al. also demonstrated the Au 3+ -containing catalyst, IRMOF-3-LA-Au, can exhibit good performance in the A 3 coupling reaction. [14] Some comparative studies have been attempted, such as the contrastive properties of gold salts and Au 0 sponges, or the activity comparison between Au NPs/PMO (PMO = periodic mesoporous organosilica) and Au(PPh 3 )Cl. [15,16] Unfortunately, these comparisons have not been able to exactly give the intrinsic property of different Au species due to the presence of different supports, which is a potential factor to affect the activity. There is still an intensive debate on the nature of the gold species involved in the reaction after the elimination of the support effect. Therefore, it is necessary to seek for a suitable model with the only difference in Au oxidation state to identify the efficient active site.As a relatively new class of crystalline porous materials, metal-organic frameworks (MOFs), featuring high porosity, structural diversity, and tailorability are attracting extensive interest and are employed toward various applications including gas storage and separation, drug delivery, sensing, catalysis, etc. [17][18][19][20][21][22][23][24][25] MOFs exhibit an unrivalled ability to realize atom-level structural determination and tailoring. Particularly, some particular functional groups with strong chelating/anchor ability can be facilely grafted onto the MOF pore walls via either onestep assembly or postsynthetic modification (PSM). [26][27][28] This character makes MOFs might be ideal supports to stabilize Au 0 and Au δ+ for studying structure-catalytic activity relationship.With the above considerations in mind, we rationally introduced the salicylaldehyde (SA) and HAuCl 4 precursors into a mesoporous MOF, MIL-101-NH 2 , via a PSM approach. SA was bound to the MOF via the reaction with the amino group to give corresponding product (denoted as MIL-101-SA) with imine As one of the most efficient catalysts for the three-component coupling reaction of aldehyde, amine, and alkyne (A 3 coupling), Au has attracted extensive attention, but there is a debating issue on whether Au δ+ (δ > 0, representing the oxidation state of Au species) or Au 0 is the better active site. According to previous reports, both Au δ+ and Au 0 can catalyze the A 3 coupling reaction. Therefore, the establishment of a suitable comparison model to identify the better active site is highly desired. In this work, an ideal m...