Unexpected crystallization of 1,3-bis(4-fluorophenyl)propan-2-one in paratone oil
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1 Acta Crystallographica Section E Structure Reports Online ISSN Editors: W. Clegg and D. G. Watson Unexpected crystallization of 1,3-bis(4-fluorophenyl)propan-2-one in paratone oil Ilia A. Guzei, Kristopher J. Kolonko and Hans J. Reich Copyright International Union of Crystallography Author(s) of this paper may load this reprint on their own web site or institutional repository provided that this cover page is retained. Republication of this article or its storage in electronic databases other than as specified above is not permitted without prior permission in writing from the IUCr. For further information see Acta Cryst. (2007). E63, o4094 Guzei et al. ffl C 15H 12 F 2 O
2 organic compounds Acta Crystallographica Section E Structure Reports Online ISSN Unexpected crystallization of 1,3-bis(4- fluorophenyl)propan-2-one in paratone oil Ilia A. Guzei,* Kristopher J. Kolonko and Hans J. Reich Department of Chemistry, University of Wisconsin Madison, 1101 University Avenue, Madison, WI 53706, USA Correspondence iguzei@chem.wisc.edu Received 12 September 2007; accepted 12 September 2007 Key indicators: single-crystal X-ray study; T = 100 K; mean (C C) = Å; R factor = 0.034; wr factor = 0.073; data-to-parameter ratio = The title compound, C 15 H 12 F 2 O, crystallizes in paratone oil as a room-temperature decomposition product of the crystalline air- and moisture-sensitive lithium enolate of 1,3-di(p-fluorophenyl)acetone diethyl ether solvate. Such spontaneous crystallization in paratone oil is rare, yet in this case it yielded X-ray quality crystals. The title compound can be prepared directly by a modified procedure of Resendiz & Garibay [Org. Lett. (2005), 7, ]. The molecular features are typical: the endocyclic angles at the electron-withdrawing F substituent average (2), while the endocyclic angles at the methylene C atom average (3). These findings are in excellent agreement with the values of and computed for the theoretically (DFT, density functional theory) optimized geometry of the title compound. Related literature Resendiz & Garibay (2005) report a direct synthesis of the title compound. Kolonko et al. (2007) report the synthesis and characterization of a Li salt that, upon decomposition, yields the title compound. For details of the software used for the computational calculations, see Frisch et al. (2004). Experimental Crystal data C 15 H 12 F 2 O M r = Orthorhombic, P a = (5) Å b = (14) Å c = (3) Å Data collection Bruker SMART 1000 CCD areadetector diffractometer Absorption correction: multi-scan SADABS (Bruker, 2007) T min = 0.950, T max = Refinement R[F 2 >2(F 2 )] = wr(f 2 ) = S = reflections V = (2) Å 3 Z =4 Mo K radiation = 0.11 mm 1 T = 100 (2) K mm measured reflections 1643 independent reflections 1210 reflections with I > 2(I) R int = parameters H-atom parameters constrained max = 0.19 e Å 3 min = 0.17 e Å 3 Data collection: SMART (Bruker, 2000); cell refinement: SAINT- Plus (Bruker, 2007); data reduction: SAINT-Plus; program(s) used to solve structure: SHELXTL (Bruker, 2007); program(s) used to refine structure: SHELXTL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL, publcif (Westrip, 2007) and modicifer (Guzei, 1995). Supplementary data and figures for this paper are available from the IUCr electronic archives (Reference: ZL2068). References Bruker (2000). SMART. Version Bruker AXS Inc., Madison, Wisconsin, USA. Bruker (2007). SADABS (Version 2007/4), SAINT-Plus (Version 7.24A) and SHELXTL (Version 6.10). Bruker AXS Inc., Madison, Wisconsin, USA. Frisch, M. J. et al. (2004). GAUSSIAN03. Revision C.02. Gaussian Inc., Wallingford, Connecticut, USA. Guzei, I. A. (1995). modicifer. University of Wisconsin Madison, USA. Kolonko, K. J., Reich, H. J., Biddle, M. & Guzei, I. A. (2007). In preparation. Resendiz, M. J. E. & Garibay, M. A. (2005). Org. Lett. 7, Westrip, S. P. (2007). publcif. In preparation. o4094 # 2007 International Union of Crystallography doi: /s Acta Cryst. (2007). E63, o4094
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