TY - JOUR
T1 - Pillararene-Based Variable Stoichiometry Co-Crystallization: A Versatile Approach to Diversified Solid-State Superstructures
AU - Li, Ming
AU - Liu, Yang
AU - Shao, Li
AU - Hua, Bin
AU - Wang, Mengbin
AU - Liang, Haozhong
AU - Khashab, Niveen M.
AU - Sessler, Jonathan L.
AU - Huang, Feihe
N1 - KAUST Repository Item: Exported on 2022-12-29
Acknowledged KAUST grant number(s): OSR-2019-CRG8-4032
Acknowledgements: F.H. thanks National Key Research and Development Program of China (2021YFA0910100), National Natural Science Foundation of China (22035006), Zhejiang Provincial Natural Science Foundation of China (LD21B020001), and the Starry Night Science Fund of Zhejiang University Shanghai Institute for Advanced Study (SN-ZJU-SIAS-006). F.H., J.L.S. and N. K. thank the King Abdullah University of Science and Technology Office of Sponsored Research (OSR-2019-CRG8-4032) for financial support. J.L.S. also acknowledges the Robert A. Foundation for chair support (F-0018). B.H. thanks the National Natural Science Foundation of China (22201252) for financial support.
PY - 2022/12/27
Y1 - 2022/12/27
N2 - Variable stoichiometry co-crystals are important in solid-state supramolecular chemistry as they allow studies of structure–property relationships while permitting the synthesis of new scaffolds using identical synthons. In this work, we extend the concept of variable stoichiometry co-crystals into the realm of pillararene chemistry and show that this permits the rational construction of a diverse set of supramolecular structures in the solid state. Specifically, we report a series of variable stoichiometry co-crystals based on pillar[n]arenes and tetracyanobenzene (TCNB) and show that the combination of in-cavity complexation by pillar[n]arenes (n = 5,6) and outside binding with TCNB allows several types of co-crystals with different self-assembled superstructures to be isolated. The variable stoichiometry co-crystals of this study display different solid-state physicochemical properties, including colors and luminescence features. Among these pillar[n]arene-based co-crystals, we discovered unique crystallographic architectures wherein two sets of individual host–guest complexes co-exist in the solid state. These mixed co-crystal systems allow for vapochromic-based detection of n-bromoalkanes. This work highlights a new strategy for the construction of self-assembled superstructures in the solid state and for tuning their intrinsic characteristics, including their luminescent and substrate-responsive features.
AB - Variable stoichiometry co-crystals are important in solid-state supramolecular chemistry as they allow studies of structure–property relationships while permitting the synthesis of new scaffolds using identical synthons. In this work, we extend the concept of variable stoichiometry co-crystals into the realm of pillararene chemistry and show that this permits the rational construction of a diverse set of supramolecular structures in the solid state. Specifically, we report a series of variable stoichiometry co-crystals based on pillar[n]arenes and tetracyanobenzene (TCNB) and show that the combination of in-cavity complexation by pillar[n]arenes (n = 5,6) and outside binding with TCNB allows several types of co-crystals with different self-assembled superstructures to be isolated. The variable stoichiometry co-crystals of this study display different solid-state physicochemical properties, including colors and luminescence features. Among these pillar[n]arene-based co-crystals, we discovered unique crystallographic architectures wherein two sets of individual host–guest complexes co-exist in the solid state. These mixed co-crystal systems allow for vapochromic-based detection of n-bromoalkanes. This work highlights a new strategy for the construction of self-assembled superstructures in the solid state and for tuning their intrinsic characteristics, including their luminescent and substrate-responsive features.
UR - http://hdl.handle.net/10754/686675
UR - https://pubs.acs.org/doi/abs/10.1021/jacs.2c11618
U2 - 10.1021/jacs.2c11618
DO - 10.1021/jacs.2c11618
M3 - Article
C2 - 36574672
SN - 0002-7863
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
ER -