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Éó¸åÈ˵ÄÕâ¾ä»°£º The conclusions should be written in an independent way to be easier for readers to follow. ʲôÒâË¼ÄØ£¿ÎÒµÄÎÄÕ conclusions ²¿·ÖÒѾÊÇÒ»¸öµ¥¶ÀµÄ¶ÎÂäÁË£¬ÔõôÓÖÊǶÀÁ¢µÄ·½Ê½ÄØ£¿ ¸½£º£¨ÎÒÊÖ¸åÖÐ conclusions ²¿·ÖµÄÈ«ÎÄ£© 4. Conclusions In preparation of new derivatives with potential biological activity, we synthesized the title derivatives with an efficient, novel and simpler procedure. The molecular structures of 1 and 2 •H2O were determined by single crystal X-ray method. Their conformations are analogous to those of some reported diarylquinolin derivatives. In spite of the aforementioned slightly conformational discrepancies, the optimized geometric bond lengths and bond angles obtained by using DFT from computational point of view are generally closer to X-ray diffraction values as seen in Table 3, which further support the solid-state structures. Henceforth, the computed results with only reasonable deviations from the experimental values seem feasible. Although the anti-tuberculosis activities are poorer than the standard drugs, the structural elucidation obtained by this paper could contribute to understanding molecular structures and especially discovering better anti-tubercular inhibitors of the substituted diarylquinoline derivatives. [ Last edited by baiyuefei on 2011-8-9 at 12:36 ] |
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snowinheart
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leimiao_hit
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leimiao_hit
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leimiao_hit
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5Â¥2011-08-09 12:50:14













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