A new 3D Pb（II） coordination polymer [Pb2（L）2（dea）]n-nH20 has been hydrothermally prepared by using the long flexible decanedioic acid （H2dea） and the N-donor chelating ligand 2-（1 H- 1,3,7,8-tetraazacyclopen...A new 3D Pb（II） coordination polymer [Pb2（L）2（dea）]n-nH20 has been hydrothermally prepared by using the long flexible decanedioic acid （H2dea） and the N-donor chelating ligand 2-（1 H- 1,3,7,8-tetraazacyclopenta[1]phenanthren-2-yl）naphthol （HL）. Single-crystal X-ray determi- nation shows that the complex crystallizes in the monoclinic system, space group C2/c with a = 25.453（5）, b = 7.5035（15）, c = 27.340（6） A, β = 114.84（3）, V = 4738.6（16） A3, Z = 8, C28H22NaOaPb, Mr = 685.69, Dc = 1.922 g/cm3, F（000） = 2656,/u（MoKa） = 7.166 mm-1, R = 0.0282 and wR = 0.0687. Two L ligands bridge two Pb（II） atoms to form a dimmer, and the neighboring dimers are further linked by the dea ligands to yield a 3D structure. The IR and TG of the compound have been investigated in detail.展开更多
The title compound, （E）-1-（7-methoxy-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl）- 3-（2-methoxyphenyl）-2-（1H-1,2,4-triazol-1-yl）propenol （3a）, was synthesized by the Aldol con- densation reaction of 1-（7-methox...The title compound, （E）-1-（7-methoxy-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl）- 3-（2-methoxyphenyl）-2-（1H-1,2,4-triazol-1-yl）propenol （3a）, was synthesized by the Aldol con- densation reaction of 1-（7-methoxy-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl）-2-（1,2,4-triazol- 1-yl）ethanone with 2-methoxybenzaldehyde and then reduced with NaBH4, and its crystal structure was determined by single-crystal X-ray diffraction： monoclinic system, space group P21 with a = 6.2002（3）, b = 12.8452（7）, c = 13.2257（7） ？, Z = 2, V = 1031.23（9） ？3, Mr = 407.46, Dc = 1.312 Mg/m3, S = 1.054, μ = 0.091 mm-1, F（000） = 432, the final R = 0.0353 and wR = 0.0769 for 3161 observed reflections （I 〉 2σ（I））. X-ray analysis displays that the title compound adopts an E configuration for the C（7）=C（8） double bond and S configuration for the chirality center with the specific rotation of –63.75°. Furthermore, the stability of the crystal was maintained through the intermolecular hydrogen bond O（1）–H？？？N（3）. The antitumor assay exhibits that the title compound 3a （E configuration） has a good antitumor activity against the Hela cell line with the IC50 value of 36.9 μM, which is better than that of 3b （Z configuration）.展开更多
基金Supported by the Jilin Province Science and Technology Development Projects (No.201105085)
文摘A new 3D Pb（II） coordination polymer [Pb2（L）2（dea）]n-nH20 has been hydrothermally prepared by using the long flexible decanedioic acid （H2dea） and the N-donor chelating ligand 2-（1 H- 1,3,7,8-tetraazacyclopenta[1]phenanthren-2-yl）naphthol （HL）. Single-crystal X-ray determi- nation shows that the complex crystallizes in the monoclinic system, space group C2/c with a = 25.453（5）, b = 7.5035（15）, c = 27.340（6） A, β = 114.84（3）, V = 4738.6（16） A3, Z = 8, C28H22NaOaPb, Mr = 685.69, Dc = 1.922 g/cm3, F（000） = 2656,/u（MoKa） = 7.166 mm-1, R = 0.0282 and wR = 0.0687. Two L ligands bridge two Pb（II） atoms to form a dimmer, and the neighboring dimers are further linked by the dea ligands to yield a 3D structure. The IR and TG of the compound have been investigated in detail.
基金Project supported by the National Natural Science Foundation of China(No.21442014)
文摘The title compound, （E）-1-（7-methoxy-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl）- 3-（2-methoxyphenyl）-2-（1H-1,2,4-triazol-1-yl）propenol （3a）, was synthesized by the Aldol con- densation reaction of 1-（7-methoxy-2,2-dimethyl-2,3-dihydrobenzofuran-5-yl）-2-（1,2,4-triazol- 1-yl）ethanone with 2-methoxybenzaldehyde and then reduced with NaBH4, and its crystal structure was determined by single-crystal X-ray diffraction： monoclinic system, space group P21 with a = 6.2002（3）, b = 12.8452（7）, c = 13.2257（7） ？, Z = 2, V = 1031.23（9） ？3, Mr = 407.46, Dc = 1.312 Mg/m3, S = 1.054, μ = 0.091 mm-1, F（000） = 432, the final R = 0.0353 and wR = 0.0769 for 3161 observed reflections （I 〉 2σ（I））. X-ray analysis displays that the title compound adopts an E configuration for the C（7）=C（8） double bond and S configuration for the chirality center with the specific rotation of –63.75°. Furthermore, the stability of the crystal was maintained through the intermolecular hydrogen bond O（1）–H？？？N（3）. The antitumor assay exhibits that the title compound 3a （E configuration） has a good antitumor activity against the Hela cell line with the IC50 value of 36.9 μM, which is better than that of 3b （Z configuration）.
