Inclusion of 1,8-octanediphosphonic acid in cucurbit[7]uril: a combined solid state and solution study

[1] Kim J(2000)New cucurbituril homologues: Syntheses, isolation, characterization, and X-ray crystal structures of cucurbit[n]uril (n = 5, 7, and 8) J. Am. Chem. Soc. 122 540-541

[2] Jung I-S(2005)Cucurbit[10]uril J. Am. Chem. Soc. 127 16798-16799

[3] Kim S-Y(2015)Cucurbiturils: From synthesis to high-affinity binding and catalysis Chem. Soc. Rev. 44 394-418

[4] Lee E(2003)Cucurbituril homologues and derivatives: New opportunities in supramolecular chemistry Acc. Chem. Res. 36 621-630

[5] Kang J-K(2007)Functionalized cucurbiturils and their applications Chem. Soc. Rev. 36 267-279

[6] Sakamoto S(2008)Cucurbit[7]uril host–guest complexes with small polar organic guests in aqueous solution Org. Biomol. Chem. 6 1796-1801

[7] Yamaguchi K(2005)Complexation of ferrocene derivatives by the cucurbit[7]uril host: A comparative study of the cucurbituril and cyclodextrin host families J. Am. Chem. Soc. 127 12984-12989

[8] Kim K(1981)Cucurbituril-based molecular recognition Cucurbituril J. Am. Chem. Soc. 103 7367-7368

[9] Liu S(2015)The potential of cucurbit[n]urils in drug delivery Chem. Rev. 115 12320-12406

[10] Zavalij PY(2011)Cucurbit[7]uril: An emerging candidate for pharmaceutical excipients Isr. J. Chem. 51 616-624

[1] Kim J(2000)New cucurbituril homologues: Syntheses, isolation, characterization, and X-ray crystal structures of cucurbit[n]uril (n = 5, 7, and 8) J. Am. Chem. Soc. 122 540-541

[2] Jung I-S(2005)Cucurbit[10]uril J. Am. Chem. Soc. 127 16798-16799

[3] Kim S-Y(2015)Cucurbiturils: From synthesis to high-affinity binding and catalysis Chem. Soc. Rev. 44 394-418

[4] Lee E(2003)Cucurbituril homologues and derivatives: New opportunities in supramolecular chemistry Acc. Chem. Res. 36 621-630

[5] Kang J-K(2007)Functionalized cucurbiturils and their applications Chem. Soc. Rev. 36 267-279

[6] Sakamoto S(2008)Cucurbit[7]uril host–guest complexes with small polar organic guests in aqueous solution Org. Biomol. Chem. 6 1796-1801

[7] Yamaguchi K(2005)Complexation of ferrocene derivatives by the cucurbit[7]uril host: A comparative study of the cucurbituril and cyclodextrin host families J. Am. Chem. Soc. 127 12984-12989

[8] Kim K(1981)Cucurbituril-based molecular recognition Cucurbituril J. Am. Chem. Soc. 103 7367-7368

[9] Liu S(2015)The potential of cucurbit[n]urils in drug delivery Chem. Rev. 115 12320-12406

[10] Zavalij PY(2011)Cucurbit[7]uril: An emerging candidate for pharmaceutical excipients Isr. J. Chem. 51 616-624