Co-crystallization of Resorcin[4]arene Tetracarboxylic Acid with Triethylamine:Synthesis and Crystal

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Treatment of resorcin[4]arene tetracarboxylic acid 1 with triethylamine in the presence of Co(CH3COO)2·4H2O and 4,4’-bipyridine gave a co-crystallization 14-·4Et3NH+(C32H20O164-·4Et3NH+,Mr=1069.27) from ethanol and water.The compound was structurally determined by single-crystal X-ray diffraction.The crystal belongs to monoclinic,space group P21/n,with a=8.1763(18),b=12.913(3),c=28.724(7) ,β=97.574(4)o,V=3006.3(12) 3,Z=2,Dc=1.181 g/cm3,F(000)=1152,Rint=0.0275,T=293(2) K,μ=0.086 mm-1,the final R=0.0634 and wR=0.1752 for 5082 observed reflections with Ⅰ > 2σ(Ⅰ).The co-crystallization is very stable at room temperature.Possibly,a network of N-H···O(=C) plays an important role in the structure.Meanwhile,the compound emits a weak cyan luminescence with peak maximum band at 458 nm. Treatment of resorcin [4] arene tetracarboxylic acid 1 with triethylamine in the presence of Co (CH3COO) 2.4H2O and 4,4’-bipyridine gave a co-crystallization 14- · 4Et3NH + (C32H20O164- · 4Et3NH +, Mr = 1069.27) from ethanol and water. The compound was structurally determined by single-crystal X-ray diffraction. The crystal belongs to monoclinic space group P21 / n with a = 8.1763 (18), b = 12.913 )  β = 97.574 (4) o V = 3006.3 (12) 3 Z = 2 Dc = 1.181 g / cm3 F000 = 1152 Rint = 0.0275 T = 293 K = μ = 0.086 mm-1, the final R = 0.0634 and wR = 0.1752 for 5082 observed reflections with I> 2σ (Ⅰ). The co-crystallization is very stable at room temperature. = C) plays an important role in the structure. Meanwhile while the compound emits a weak cyan luminescence with peak maximum band at 458 nm.
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