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

[11] Isaacs L(2017)Methods of crystallochemical analysis of supramolecular complexes by means of Voronoi-Dirichlet polyhedra: A study of cucurbituril host-guest compounds Ann. N Y Acad. Sci. 1398 108-119

[12] Assaf KI(2004)Strong binding of hydrocarbons to cucurbituril probed by fluorescent dye displacement: A supramolecular gas-sensing ensemble Acta Crystallogr. Sect. B 60 350-357

[13] Nau WM(2011)Binding affinities of cucurbit[n]urils with cations Angew Chem. Int. Ed. 50 9338-9342

[14] Lee JW(2019)Cucurbit[n]uril-based coordination chemistry: From simple coordination complexes to novel poly-dimensional coordination polymers Chem. Commun. 55 14131-14134

[15] Samal S(2013)Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant Chem. Soc. Rev. 42 9480-9508

[16] Selvapalam N(2014)Deep inside cucurbiturils: Physical properties and volumes of their inner cavity determine the hydrophobic driving force for host–guest complexation Angew Chem. Int. Ed. 53 988-993

[17] Kim H-J(2011)Metal–organic frameworks for separations Isr. J. Chem. 51 559-577

[18] Kim K(2012)Macrocyclic Cu(II)-organophosphonate building block with room temperature magnetic ordering Chem. Rev. 112 869-932

[19] Kim K(2015)Mimicking cellular phospholipid bilayer packing creates predictable crystalline molecular metal–organophosphonate macrocycles and cages Dalton Trans. 44 12526-12529

[20] Selvapalam N(2018)Conventional and unconventional metal–organic frameworks based on phosphonate ligands: MOFs and UMOFs CrystEngComm 20 2152-2158

[11] Isaacs L(2017)Methods of crystallochemical analysis of supramolecular complexes by means of Voronoi-Dirichlet polyhedra: A study of cucurbituril host-guest compounds Ann. N Y Acad. Sci. 1398 108-119

[12] Assaf KI(2004)Strong binding of hydrocarbons to cucurbituril probed by fluorescent dye displacement: A supramolecular gas-sensing ensemble Acta Crystallogr. Sect. B 60 350-357

[13] Nau WM(2011)Binding affinities of cucurbit[n]urils with cations Angew Chem. Int. Ed. 50 9338-9342

[14] Lee JW(2019)Cucurbit[n]uril-based coordination chemistry: From simple coordination complexes to novel poly-dimensional coordination polymers Chem. Commun. 55 14131-14134

[15] Samal S(2013)Cucurbit[7]uril⋅guest pair with an attomolar dissociation constant Chem. Soc. Rev. 42 9480-9508

[16] Selvapalam N(2014)Deep inside cucurbiturils: Physical properties and volumes of their inner cavity determine the hydrophobic driving force for host–guest complexation Angew Chem. Int. Ed. 53 988-993

[17] Kim H-J(2011)Metal–organic frameworks for separations Isr. J. Chem. 51 559-577

[18] Kim K(2012)Macrocyclic Cu(II)-organophosphonate building block with room temperature magnetic ordering Chem. Rev. 112 869-932

[19] Kim K(2015)Mimicking cellular phospholipid bilayer packing creates predictable crystalline molecular metal–organophosphonate macrocycles and cages Dalton Trans. 44 12526-12529

[20] Selvapalam N(2018)Conventional and unconventional metal–organic frameworks based on phosphonate ligands: MOFs and UMOFs CrystEngComm 20 2152-2158