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3 (0.0583 g), DLcamphoric acid (0.1037 g), and triethanolamine (1.9582 g) were mixed in a 23-mL Teflon cup, and the mixture was stirred for 20 min. The vessel was then sealed and heated at 140 °C for 5 days. The autoclave was subsequently allowed to cool to room temperature. Transparent colorless crystals were obtained. The homochiral form Zn(△-Zn(Htea))(D-cam) (1D△) or 1L△ can be obtained by using a similar reaction except D-camphoric acid (or L-camphoric acid) instead of DL-camphoric acid was used.
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3 (0.0583 g), DLcamphoric acid (0.1037 g), and triethanolamine (1.9582 g) were mixed in a 23-mL Teflon cup, and the mixture was stirred for 20 min. The vessel was then sealed and heated at 140 °C for 5 days. The autoclave was subsequently allowed to cool to room temperature. Transparent colorless crystals were obtained. The homochiral form Zn(△-Zn(Htea))(D-cam) (1D△) or 1L△ can be obtained by using a similar reaction except D-camphoric acid (or L-camphoric acid) instead of DL-camphoric acid was used.
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Crystal data for 1DA: C16H27NZn 2O7, Mr, 476.13, orthorhombic, space group P212121, a, 12.1362(11)Å, b, 12.2752(16)Å, c, 12.7945(14) A, V= 1906.1(4) Å3, Z, 4, Flack parameter, 0.01(6, R1 (wR2, 0.0768 (0.1782, and S, 1.087 for 1618 reflections with I > 2σ(I, Crystal data for 1L△: C16H 27NZn2O7, Mr, 476.13, orthorhombic, space group P2121,21a, 12.1540(5) Å, 12.3292(7) Å,c=12.8100(8)Å, K= 1919.57(18)Å3, Z, 4, Flack parameter, 0.06(4, R1 (wR2, 0.0665 (0.1652, and S, 0.985 for 1809 reflections with I > 2σI, The structure was solved by direct methods followed by successive difference Fourier methods. Computations were performed
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