The curious case of (caffeine)•(benzoic acid): how heteronuclear seeding allowed the formation of an elusive cocrystal

被引:119
作者
Bucar, Dejan-Kresimir [1 ]
Day, Graeme M. [2 ]
Halasz, Ivan [3 ,4 ]
Zhang, Geoff G. Z. [5 ]
Sander, John R. G. [6 ]
Reid, David G. [1 ]
MacGillivray, Leonard R. [6 ]
Duer, Melinda J. [1 ]
Jones, William [1 ]
机构
[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
[2] Univ Southampton, Sch Chem, Southampton SO17 1BJ, Hants, England
[3] Univ Zagreb, Fac Sci, Dept Chem, Zagreb 10002, Croatia
[4] Rudjer Boskovic Inst, Div Mat Chem, Zagreb 10002, Croatia
[5] AbbVie Inc, Res & Dev, N Chicago, IL 60064 USA
[6] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
基金
英国生物技术与生命科学研究理事会;
关键词
SOLID-STATE; PHARMACEUTICAL COCRYSTALS; CO-CRYSTALS; CAFFEINE; POLYMORPHS; LUMINESCENT; PREDICTION; RITONAVIR;
D O I
10.1039/c3sc51419f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Cocrystals are modular multicomponent solids with exceptional utility in synthetic chemistry and materials science. A variety of methods exist for the preparation of cocrystals, yet, some promising cocrystal phases have proven to be intractable synthetic targets. We describe a strategy for the synthesis of the pharmaceutically relevant (caffeine).(benzoic acid) cocrystal (1), which persistently failed to form using a broad range of established techniques. State-of-the-art crystal structure prediction methods were employed to assess the possible existence of a thermodynamically stable form of 1, hence to identify appropriate heteronuclear seeds for cocrystallization. Once introduced, the designed heteronuclear seeds facilitated the formation of 1 and, significantly they (or seeds of the product cocrystal) continued to act as long-lasting laboratory "contaminants", which encouraged cocrystal formation even when present at such low levels as to evade detection. The seeding technique described thus enables the synthesis of cocrystals regarded as unobtainable under desired conditions, and potentially signifies a new direction in the field of materials research.
引用
收藏
页码:4417 / 4425
页数:9
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