[1] Batten, S. R., Neville, S. M., Turner, D. R., “Coordination polymers: design, analysis and application” Royal Society of Chemistry: Cambridge, U.K.: (2009).
[2] Kitagawa, S., Kitaura, R., Noro, S., “Functional porous coordination polymers” Angew. Chem. Int. Ed., 43 (2004) 2334-2375.
[3] Notash, B., Zolfaghari, M., Mir Mohammad Sadegh, B., “Synthesis, Characterization and Determination of the Crystal Structure of New Cadmium Coordination Polymers Based on Bridging Schiff-Base Pyridine Ligand; Investigation of Hirshfeld Surface Analysis (in Persian)” M. J. Appl. Chem., 15 (2020) 95-110.
[4] Notash, B., “Synthesis, Characterization and Crystal Structure Determination of New Coordination Polymers of Cadmium (II) Based on Pyridine Hydrazide Ligands (in Persian)” Iran J. Cryst. Miner., 26 (2019) 1001-1012.
[5] Wang, H. N., Meng, X., Dong, L. Z., Chen, Y., Li, S. L., Lan, Y. Q., “Coordination polymer-based conductive materials: ionic conductivity vs. electronic conductivity” J. Mater. Chem. A, 7 (2019) 24059-24091.
[6] Seguin, A. K., Cruz, C., Villafuerte, K., Páez-Hernández, D., Venegas-Yazigi, D., Paredes-García, V., “One-Dimensional CoII and NiII Helical Coordination Polymers Exhibiting Zero-Field Splitting” Cryst. Growth Des., 23 (2023) 77-86.
[7] Movilla, F., Rey, J. M., Saleta, M. E., Gonzaléz-Carvajal, M., Spodine, E., Cancino, P., Di Salvo, F., “Phenylalanine-Based Co2+ and Cd2+ 1D Coordination Polymers: Structural Properties and Catalytic Application for Solvent-Free Aerobic Oxidation of Cycloalkene” Inorg. Chem., 62 (2023) 17136-17149.
[8] Tang, J., Shen, Y., He, X., Chen, M., Zhao, H., Wang, Y., Jiang, J., Liu, P., Dang, R., Zhang, M., Qin, G., Bai, J., Duan, J., “Tuning Multiple Counter-Anions in Porous Coordination Polymers with lcy Topology for Acetylene/Ethylene Separation” Inorg. Chem., 63 (2024) 3667-3674.
[9] Shit, M., Halder, S., Manna, K., Karan, A. K., Samanta, A., Manik, N. B., Pal, S., Jana, K., Sinha, C., “Mn(II) 3D Coordination Framework with Mixed 5-Aminoisophthalato and Pyridyl-isonicotinoyl Hydrazone Bridges: Structure, Electrical Conductivity, Anticancer Activity, and Drug Delivery” ACS Appl. Polym. Mater., 6 (2024) 2637-2648.
[10] Lawson, H. D., Walton, S. P., Chan, C., “Metal–Organic Frameworks for Drug Delivery: A Design Perspective” ACS Appl. Mater. Interfaces, 13 (2021) 7004-7020.
[11] Zheng, H., Zhang, Y., Liu, L., Wan, W., Guo, P., Nyström, A. M., Zou, X., “One-pot Synthesis of Metal–Organic Frameworks with Encapsulated Target Molecules and Their Applications for Controlled Drug Delivery” J. Am. Chem. Soc., 138 (2016) 962-968.
[12] Carmona-Sarabia, L., Quiñones Vélez, G., Escalera-Joy, A. M., Mojica-Vázquez, D., Esteves-Vega, S., Peterson-Peguero, E. A., López-Mejías, V., “Design of Extended Bisphosphonate-Based Coordination Polymers as Bone-Targeted Drug Delivery Systems for Breast Cancer-Induced Osteolytic Metastasis and Other Bone Therapies” Inorg. Chem., 62 (2023) 9440-9453.
[13] Mandal, J., Dey, A., Sarkar, S., Khatun, M., Ghorai, P., Ray, P. P., Mahata, P., Saha, A., “Chromone-Based Cd(II) Fluorescent Coordination Polymer Fabricated to Study Optoelectronic and Explosive Sensing Properties” Inorg. Chem., 63 (2024) 4527-4544.
[14] Datta, S., Dey, S., Sinha, C., Dutta, B., Banerjee, P., Mir, M. H., “Exploitation of a 1D coordination polymer as a portable kit for an eye-catching fluorometric response towards sensing of trivalent cations” Dalton Trans., 53 (2024) 2859-2866.
[15] Li, S.-Q., Zhao, F.-H., Li, Z.-L., Wu, X.-H., “Modulated Synthesis of Two Fluorescent Zn(II)–Eu(III) Bimetallic Coordination Polymers for Sensing of Vanillin and Folic Acid” Cryst. Growth Des., 25 (2025) 6940-6953.
[16] Liu, M., Quah, H. S., Wen, S., Wang, J., Kumar, P. S., Eda, G., Vittal, J. J., Ji, W., “Nonlinear optical properties of a one-dimensional coordination polymer” J. Mater. Chem. C, 5 (2017) 2936-2941.
[17] Geng, K., Yang, X., Zhao, Y., Cui, Y., Ding, J. Hou, H., “Efficient strategy for investigating the third-order nonlinear optical (NLO) properties of solid-state coordination polymers” Inorg. Chem., 61 (2022) 12386-12395.
[18] Liu, R. Q., Zhao, N., Yang, F.-X., Wang, A.-R., Liu, P., An, C.-X. Lian, Z.-X., “Enhanced third-order nonlinear optical properties of three 2D coordination polymers based on bis (imidazole) ligands and dicarboxylic ligands” Polyhedron, 111 (2016) 16-25.
[19] Hay, B. P., Custelcean, R., “Anion−π interactions in crystal structures: commonplace or extraordinary?” Cryst. Growth Des., 9 (2009) 2539-2545.
[20] Dawson, R. E., Hennig, A., Weimann, D. P., Emery, D., Ravikumar, V., Montenegro, J., Takeuchi, T., Gabutti, S., Mayor, M., Mareda, J. Schalley, C. A., “Experimental evidence for the functional relevance of anion–π interactions” Nat. chem., 2 (2010) 533-538.
[21] Frontera, A., Gamez, P., Mascal, M., Mooibroek, T. J. Reedijk, J., “Putting anion–π interactions into perspective” Angew. Chem. Int. Ed., 50 (2011) 9564-9583.
[22] Robertazzi, A., Krull, F., Knapp, E. W. Gamez, P., “Recent advances in anion–π interactions” CrystEngComm, 13 (2011) 3293-3300.
[23] Ebrahimi, B., Notash, B., Matar, T., Dinnebier, R., “In Situ Conversion of Ligand to a Coordination Polymer via a Core@Shell Crystal: A Multi-Step Phase-Dependent Structural Transformation” Inorg. Chem., 63 (2024) 983-999.
[24] Ebrahimi, B., Notash, B., “Facile fabrication in coordination networks: an in situ sequential replacement of linkers by successive SC–SC transformations via core@shell crystals” CrystEngComm, 26 (2024) 4720-4731.
[25] Quiñonero, D., Garau, C., Rotger, C., Frontera, A., Ballester, P., Costa, A., Deyà, P. M., “Anion–π Interactions: Do They Exist?” Angew. Chem. Int. Ed., 41 (2002) 3389-3392.
[26] Alkorta, I., Rozas, I., Elguero, J., “Interaction of Anions with Perfluoro Aromatic Compounds” J. Am. Chem. Soc., 124 (2002) 8593-8598.
[27] Mascal, M., Armstrong, A., Bartberger, M. D., “Anion−Aromatic Bonding: A Case for Anion Recognition by π-Acidic Rings” J. Am. Chem. Soc., 124 (2002) 6274-6276.
[28] Fang, X., Yuan, X., Song, Y. B., Wang, J. D., Lin, M. J., “Cooperative lone pair–π and coordination interactions in naphthalene diimide coordination networks” CrystEngComm, 16 (2014) 9090-9095.
[29] You, M. H., Li, M. H., Liu, Y. F., Li, H. H., Lin, M. J., “Unprecedented five-fold interpenetrated donor–acceptor hybrid heterostructure induced by anion–π interactions” CrystEngComm, 21 (2019) 6688-6692.
[30] Kobylarczyk, J., Pinkowicz, D., Srebro-Hooper, M., Hooper, J. Podgajny, R., “Anion-π architectures of HAT(CN)6 and 5d polycyanidometalates:[W(CN)8]3–,[Re(CN)7]3–, and [Pt(CN)6]2–” Cryst. Growth Des., 19 (2018) 1215-1225.
[31] Gordillo, M. A., Benavides, P. A., Saha, S., “Anion/Naphthalenediimide Interactions in a Pd (II)-Based Tetrameric Metallocycle” Cryst. Growth Des., 19 (2019) 6017-6022.
[32] Berdiell, I. C., Farmiloe, S. E., Kulmaczewski, R., Halcrow, M. A., “Molecular squares, coordination polymers and mononuclear complexes supported by 2, 4-dipyrazolyl-6 H-1, 3, 5-triazine and 4, 6-dipyrazolylpyrimidine ligands” Dalton Trans., 48 (2019) 17310-17320.
[33] Savastano, M., Bazzicalupi, C., Giorgi, C., García-Gallarín, C., López De La Torre, M. D., Pichierri, F., Bianchi, A., Melguizo, M., “Anion complexes with tetrazine-based ligands: formation of strong anion−π interactions in solution and in the solid state” Inorg. Chem., 55 (2016) 8013-8024.
[34] Mahajan S., Marttinen A., Forsblom S., Lahtinen M., “Inorganic Anion-Mediated Supramolecular Entities of 4-Amino-3,5-Bis(4-Pyridyl)-1,2,4-Triazole Salts Assisted by the Interplay of Noncovalent Interactions” Cryst. Growth Des., 23 (2023) 5144-5162.
[35] Patnaik P., “Dean’s Analytical Chemistry Handbook” 2nd ed.; McGraw-Hill Education: New York, (2004).
[36] Mooibroek, T. J., Black, C. A., Gamez, P., Reedijk, J., “What’s new in the realm of anion−π binding interactions? Putting the anion−π interaction in perspective” Cryst. Growth Des., 8 (2008) 1082-1093.
[37] Spackman, M. A., Jayatilaka, D., “Hirshfeld surface analysis” CrystEngComm, 11 (2009) 19-32.
[38] Spackman, M. A., McKinnon, J. J., “Fingerprinting intermolecular interactions in molecular crystals” CrystEngComm, 4 (2002) 378-392.
[39] Notash, B., “1D helical cadmium coordination polymers containing hydrazide ligand: The role of solvent and molar ratio” J. Mol. Struct., 1156 (2018) 534-543.
[40] Ebrahimi, B., Notash, B., “Moisture-induced single-crystal-to-powder structural transformation in cadmium coordination compounds containing electron-deficient ligand: coordinated solvent exchange and retention of dimension” CrystEngComm, 27 (2025) 5889-5900.