1. (a) Huck, W. T. S. et al. Noncovalent Synthesis of Nanostructures: Combining Coordination Chemistry and Hydrogen Bonding. Angew. Chem. Int. Ed. Engl. 36, 1006 – 1008 (1997); (b) Goral, V. et al. Double-level “orthogonal” dynamic combinatorial libraries on transition metal template. Proc. Natl. Acad. Sci. USA, 98, 1347 – 1352 (2001); (c) Saha, M. L. et al. Orthogonality in discrete self-assembly – survey of current concepts. Chem. Soc. Rev. 42, 6860 – 6909 (2013); (d) Hu, X.-Y. et al. Dynamic Supramolecular Complexes Constructed by Orthogonal Self-Assembly. Acc. Chem. Res. 47, 2041 – 2051 (2014); (e) Wilson, A. et al. Functional systems with orthogonal dynamic covalent bonds. Chem. Soc. Rev. 43, 1948 – 1962 (2014); (f) Wei, P. et al. Supramolecular polymers constructed by orthogonal self-assembly based on host–guest and metal–ligand interactions. Chem. Soc. Rev. 44, 815-832 (2015); (g) Lu, C. et al. Fluorescent Metallacage-Core Supramolecular Polymer Gel Formed by Orthogonal Metal Coordination and Host–Guest Interactions. J. Am. Chem. Soc. 140, 7674 – 7680 (2018); (h) Zhang, Q. et al. Self-Healing Heterometallic Supramolecular Polymers Constructed by Hierarchical Assembly of Triply Orthogonal Interactions with Tunable Photophysical Properties. J. Am. Chem. Soc. 141, 17909−17917 (2019).
2. (a) Kramer, R. et al. Self-recognition in helicate self-assembly: spontaneous formation of helical metal complexes from mixtures of ligands and metal ions. Proc. Natl. Acad. Sci. USA 90, 5394 – 5398 (1993); (b) Rowan, S. J. et al. Automated Recognition, Sorting, and Covalent Self-Assembly by Predisposed Building Blocks in a Mixture. J. Am. Chem. Soc. 119, 2578 – 2579 (1997); (c) Wu, A. et al. Self-Sorting: The Exception or the Rule. J. Am. Chem. Soc. 125, 4831 – 4835 (2003); (d) He, Z. et al. Integrative self-sorting: a versatile strategy for the construction of complex supramolecular architecture. Chem. Soc. Rev. 44, 779 – 789 (2015); (e) Wang, W. et al. Supramolecular transformations within discrete coordination-driven supramolecular architectures. Chem. Soc. Rev. 45, 2656 – 2693 (2016); (f) Saha, S. et al. Structure relationships between bis-monodentate ligands and coordination driven self-assemblies. Coord. Chem. Rev. 374, 1 – 14 (2018).
3. (a) Acharyya, K. et al. Molecular Marriage through Partner Preferences in Covalent Cage Formation and Cage-to-Cage Transformation. J. Am. Chem. Soc. 135, 554 –557 (2013); (b) Gidron, O. et al. Homochiral [2]Catenane and Bis[2]catenane from Alleno-AcetylenicHelicates - A Highly Selective Narcissistic Self-Sorting Process. J. Am. Chem. Soc. 137, 12502–12505 (2015); (c) Beaudoin, D. et al. Chiral Self-Sorting of [2+3] Salicylimine Cage Compounds. Angew. Chem. Int. Ed. 56, 1244–1248 (2017); (d) Wang, X. et al. Narcissistic chiral self-sorting of molecular face-rotating polyhedral. Org. Biomol. Chem. 16, 34– 37 (2018); (e) Kołodziejski, M. et al. Dynamic polyimine macrobicyclic cryptands – self-sorting with component selection. Chem. Sci. 10, 1836–1843 (2019); (f) Zhao, X. et al. Narcissistic self-sorting in anion-coordination-driven assemblies. Chem. Commun., 57, 6078–6081 (2021).
4. (a) Mukhopadhyay, P. et al. Social Self-Sorting in Aqueous Solution. J. Org. Chem. 69, 6157–6164 (2004); (b) Tomimasu, N. et al. Social Self-Sorting: Alternating Supramolecular Oligomer Consisting of Isomers. J. Am. Chem. Soc. 131, 12339–12343 (2009); (c) Joseph, R. et al. Stabilization of Cucurbituril/Guest Assemblies via Long-Range Coulombic and CH···O Interactions. J. Am. Chem. Soc. 136, 6602–6607 (2014); (d) Klotzbach, S. et al. Shape-Controlled Synthesis and Self-Sorting of Covalent Organic Cage Compounds. Angew. Chem. Int. Ed. 54, 10356 – 10360 (2015); (e) Beuerle, F. et al. Let’s Sort It Out: Self-Sorting of Covalent Organic Cage Compounds. Synlett 27, 1133–1138 (2016); (f) Greenaway, R. L. et al. From Concept to Crystals via Prediction: Multi-Component Organic Cage Pots by Social Self-Sorting. Angew. Chem. Int. Ed. 58, 16275 –16281 (2019); (g) Abet, V. et al. Inducing Social Self-Sorting in Organic Cages To Tune The Shape of The Internal Cavity. Angew. Chem. Int. Ed. 59, 16755 – 16763 (2020).
5. Meyer, C. D. et al. Template-directed synthesis employing reversible imine bond formation. Chem. Soc. Rev. 36, 1705 – 1723 (2007).
6. (a) Baxter, P. N. W. et al. Multicomponent Self-Assembly: Spontaneous Formation of a Cylindrical Complex from Five Ligands and Six Metal Ions. Angew. Chem. Int. Ed. Engl. 32, 69 – 72 (1993); (b) Caulder, D. L. et al. Superamolecular Self-Recognition and Self-Assembly in Gallium(III) Catecholamide Triple Helices. Angew. Chem. Int. Ed. Engl. 36, 1440 – 1442 (1997); (c) Taylor, P. N. et al. Cooperative Self-Assembly of Double-Strand Conjugated Porphyrin Ladders. J. Am. Chem. Soc. 121, 11538 – 11545 (1999); (d) Ibukuro, F. et al. Quantitative and Spontaneous Formation of a Doubly Interlocking [2]Catenane Using Copper(I) and Palladium(II) as Templating and Assembling Centers. J. Am. Chem. Soc. 121, 11014 – 11015 (1999); (e) Schultz, D. et al. Choices of Iron and Copper: Cooperative Selection during Self-Assembly. Angew. Chem. Int. Ed. 45, 2453 – 2456 (2006); (f) Mahata, K. et al. From 2-Fold Completive to Integrative Self-Sorting: A Five-Component Supramolecular Trapezoid. J. Am. Chem. Soc. 131, 16544 – 16554 (2009); (g) Zheng, Y. R. et al. Multicomponent Supramolecular Systems: Self-Organization in Coordination-Driven Self-Assembly. Chem. Eur. J. 15, 7203 – 7214 (2009); (h) Schmittel, M. et al. Scaffolding a Cage-Like 3D Framework by Coordination and Constitutional Dynamic Chemistry. Org. Lett. 13, 3916 – 3919 (2011); (i) Campbell, C. J. et al. A Simple and Highly Effective Ligand System for the Copper(I)-Mediated Assembly of Rotaxanes. Angew. Chem. Int. Ed. 53, 13771 – 13774 (2014); (j) Lu, X. et al. Probing a Hidden World of Molecular Self-Assembly: Concentration-Dependent, Three-Dimensional Supramolecular Interconversions. J. Am. Chem. Soc. 136, 18149 – 18155 (2014); (k) Ramsay, W. J. et al. Designed Enclosure Enables Guest Binding Within the 4200 Å3 Cavity of a Self-Assembled Cube. Angew. Chem. Int. Ed. 54, 5636 – 5640 (2015); (l) Gidron, O. et al. Homochiral [2]Catenane and Bis[2]catenane from Alleno-Acetylenic Helicates - A Highly Selective Narcissistic Self-Sorting Process. J. Am. Chem. Soc. 137, 12502−12505 (2015); (m) Bloch, W. M. et al. Morphological Control of Heteroleptic cis- and trans-Pd2L2L′2 Cages. Angew. Chem.Int. Ed. 56, 8285 – 8289 (2017); (n) Sepehrpour, H. et al. Fe–Pt Twisted Heterometallic Bicyclic Supramolecules via Multicomponent Self-Assembly. J. Am. Chem. Soc. 139, 2553 – 2556 (2017); (o) Gaikwad, S. et al. Five-component trigonal nanoprism with six dynamic corners. Chem. Commun. 53, 8034 – 8037 (2017); (p) Rizzuto, F. J. et al. Otherwise Unstable Structures Self-Assemble in the Cavities of Cuboctahedral Coordination Cages. J. Am. Chem. Soc. 140, 11502 – 11509 (2018); (q) Ayme, J.-F. et al. Inside Cover: Synergistic N-Heterocyclic Carbene/Palladium-Catalyzed Umpolung 1,4-Addition of Aryl Iodides to Enals. Angew.Chem. Int. Ed. 59, 2 – 11 (2020).
7. (a) Otto, S. et al. Selection and Amplification of Hosts From Dynamic Combinatorial Libraries of Macrocyclic Disulfides. Science 297, 590-593 (2002); (b) Sadownik, J.W. et al. A Simple Synthetic Replicator Amplifies Itself from a Dynamic Reagent Pool. Angew.Chem. Int. Ed. 47, 9965 – 9970 (2008); (c) Vongvilai, P. et al. Dynamic Asymmetric Multicomponent Resolution: Lipase-Mediated Amidation of a Double Dynamic Covalent System. J. Am. Chem. Soc. 131, 14419 – 14425 (2009); (d) Ajami, D. et al. Compressed alkanes in reversible encapsulation complexes. Nat. Chem. 1, 87 – 90 (2009); (e) Osowska, K. et al. Oxidative Kinetic Self-Sorting of a Dynamic Imine Library. J. Am. Chem. Soc. 133, 724–727 (2011); (f) Jiang, W. et al. Guest-Induced, Selective Formation of Isomeric Capsules with Imperfect Walls. J. Am. Chem. Soc. 134, 17498−17501 (2012); (g) Ji, Q. et al. Distillative Self-Sorting of Dynamic Ester Libraries. J. Org. Chem. 78, 12710−12716 (2013); (h) Klotzbach, S. et al. Shape-Controlled Synthesis and Self-Sorting of Covalent Organic Cage Compounds. Angew.Chem. Int. Ed. 54, 10356 – 10360 (2015).
8. Jiao, T. et al. Self-Assembly in Water with N-Substituted Imines. Angew.Chem. Int. Ed. 59, 18350 –18367 (2020).
9. (a) Li, H. et al. Quantitative self-assembly of a purely organic three-dimensional catenane in water. Nat. Chem. 7, 1003 – 1008 (2015). (b) Zheng, X. et al. Temperature-dependent self-assembly of a purely organic cage in water. Chem. Commun. 54, 3138 –3141 (2018); (c) Zhang, Y. et al. A Kinetically Stable Macrocycle Self-Assembled in Water. Org. Lett. 20, 2356 – 2359 (2018); (d) Wu, G. et al. Controllable Self-Assembly of Macrocycles in Water for Isolating Aromatic Hydrocarbon Isomers. J. Am. Chem. Soc. 140, 5955 – 5961 (2018); (e) Wang, C.-Y. et al. Precursor control over the self-assembly of [2]catenanes via hydrazone condensation in water. Chem. Commun. 54, 5106 – 5109 (2018); (f) Chen, Q. et al. Ultramacrocyclization via selective catenation in water.Chem. Commun. 55, 13108 – 13111 (2019).
10. (a) Cougnon, F. B. L. et al. A Strategy to Synthesize Molecular Knots and Links Using the Hydrophobic Effect. J. Am. Chem. Soc. 140, 12442 – 12450 (2018); (b) Caprice, K. et al. Synchronized On/Off Switching of Four Binding Sites for Water in a Molecular Solomon Link. Angew. Chem. Int. Ed. 58, 8053 – 8057 (2019); (c) Kruve, A. et al. Ion-Mobility Mass Spectrometry for the Rapid Determination of theTopology of Interlocked and Knotted Molecules. Angew. Chem. Int. Ed. 58, 11324 – 11328 (2019); (d) Neira, I. et al. Adjusting the Dynamism of Covalent Imine Chemistry in the Aqueous Synthesis of Cucurbit[7]uril-based [2]Rotaxanes. Org. Lett. 21, 8976 – 8980 (2019); (e) Blanco-Gómez, A. et al. Thinking Outside the “Blue Box”: Induced Fit within a Unique Self-Assembled Polycationic Cyclophane. J. Am. Chem. Soc. 141, 3959 – 3964 (2019); (f) Caprice, K. et al. Untying the Photophysics of Quinolinium-Based Molecular Knots and Links. Chem. Eur. J. 26, 1576 –1587 (2020).
11. (a) Zhang, Z.‐Y. et al. Efficient Room-Temperature Phosphorescence of a Solid-State Supramolecule Enhanced by Cucurbit[6]uril. Angew. Chem. Int. Ed. 58, 6028–6032 (2019); (b) Zhang, Z.‐Y. et al. Ultralong room-temperature phosphorescence of a solid-state supramolecule between phenylmethylpyridinium and cucurbit[6]uril. Chem. Sci. 10, 7773 – 7778 (2019); (c) Zhang, Z.‐Y. et al. Inside Cover: Synergistic N-Heterocyclic Carbene/Palladium-Catalyzed Umpolung 1,4-Addition of Aryl Iodides to Enals. Angew. Chem. Int. Ed. 59, 2–9 (2020).
12. (a) Wu, H. et al. Ring-in-Ring(s) Complexes Exhibiting Tunable Multicolor Photoluminescence. J. Am. Chem. Soc. 142, 16849−16860 (2020); (b) Shen, F.-F. et al. Purely organic light-harvesting phosphorescence energy transfer by b-cyclodextrin pseudorotaxane for mitochondria targeted imaging.Chem. Sci. 12, 1851–1857 (2020); (c) Ma, X.-K. et al. Supramolecular Pins with Ultralong Efficient Phosphorescence. Adv. Mater. 33, 2007476 (2021).
13. Mei, J. et al. Aggregation-Induced Emission: Together We Shine, United We Soar! Chem. Rev. 115, 11718 −11940 (2015).