TY - JOUR
T1 - Multicomponent, Multicavity Metallacages That Contain Different Binding Sites for Allosteric Recognition
AU - Liu, Haifei
AU - Guo, Chenxing
AU - Li, Luqi
AU - Zhang, Zeyuan
AU - Hou, Yali
AU - Mu, Chaoqun
AU - Hou, Gao Lei
AU - Zhang, Zhenyi
AU - Wang, Heng
AU - Li, Xiaopeng
AU - Zhang, Mingming
N1 - Publisher Copyright:
© 2024 American Chemical Society
PY - 2024/6/12
Y1 - 2024/6/12
N2 - The encapsulation of different guest molecules by their different recognition domains of proteins leads to selective binding, catalysis, and transportation. Synthetic hosts capable of selectively binding different guests in their different cavities to mimic the function of proteins are highly desirable but challenging. Here, we report three ladder-shaped, triple-cavity metallacages prepared by multicomponent coordination-driven self-assembly. Interestingly, the porphyrin-based metallacage is capable of heteroleptic encapsulation of fullerenes (C60 or C70) and coronene using its different cavities, allowing distinct allosteric recognition of coronene upon the addition of C60 or C70. Owing to the different binding affinities of the cavities, the metallacage hosts one C60 molecule in the central cavity and two coronene units in the side cavities, while encapsulating two C70 molecules in the side cavities and one coronene molecule in the central cavity. The rational design of multicavity assemblies that enable heteroleptic encapsulation and allosteric recognition will guide the further design of advanced supramolecular constructs with tunable recognition properties.
AB - The encapsulation of different guest molecules by their different recognition domains of proteins leads to selective binding, catalysis, and transportation. Synthetic hosts capable of selectively binding different guests in their different cavities to mimic the function of proteins are highly desirable but challenging. Here, we report three ladder-shaped, triple-cavity metallacages prepared by multicomponent coordination-driven self-assembly. Interestingly, the porphyrin-based metallacage is capable of heteroleptic encapsulation of fullerenes (C60 or C70) and coronene using its different cavities, allowing distinct allosteric recognition of coronene upon the addition of C60 or C70. Owing to the different binding affinities of the cavities, the metallacage hosts one C60 molecule in the central cavity and two coronene units in the side cavities, while encapsulating two C70 molecules in the side cavities and one coronene molecule in the central cavity. The rational design of multicavity assemblies that enable heteroleptic encapsulation and allosteric recognition will guide the further design of advanced supramolecular constructs with tunable recognition properties.
UR - https://www.scopus.com/pages/publications/85193270253
U2 - 10.1021/jacs.4c01873
DO - 10.1021/jacs.4c01873
M3 - 文章
C2 - 38738985
AN - SCOPUS:85193270253
SN - 0002-7863
VL - 146
SP - 15787
EP - 15795
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 23
ER -