馮秀玲, 張玉平
(懷化學(xué)院 化學(xué)化工系,湖南 懷化 418008)
金屬-有機(jī)超分子化合物因其新穎的結(jié)構(gòu)在分子識(shí)別、選擇性催化、非線性光學(xué)材料、醫(yī)藥等領(lǐng)域展示出了潛在的應(yīng)用前景[1,2]。這些化合物大多是用剛性或柔性的有機(jī)配體與過(guò)渡金屬元素通過(guò)較強(qiáng)的配位鍵或較弱的作用力,如氫鍵和π-π堆積作用形成一維、二維或三維等多種拓?fù)浣Y(jié)構(gòu)[3~5]。氫鍵作為一種重要的分子間弱相互作用,它的存在不僅能使化合物結(jié)構(gòu)更穩(wěn)定、分子體系能量降低,還能使配合物的物理、化學(xué)性質(zhì)發(fā)生明顯的變化, 進(jìn)而改變其光、電、磁等性質(zhì)[6~8]。
本文以Co(NO3)2·6H2O,鄰菲啰啉(phen)與L-丙氨酸(L-alanato)為原料,通過(guò)水熱法合成了新型超分子化合物[Co(L-alanato)2(phen)]NO3·4H2O(1),其結(jié)構(gòu)經(jīng)IR,元素分析和X-射線單晶衍射分析表征。
Nicolet 170SX FT-IR型傅立葉紅外光譜儀(KBr壓片);Carlo Erba 1106型元素分析儀;Mettler Toledo TGA/SDTA 851型熱重分析儀;Bruker Smart APEXⅡ型X-射線單晶衍射儀。
所用試劑均為分析純。
在內(nèi)襯聚四氟乙烯的不銹鋼反應(yīng)釜中依次加入Co(NO3)2·6H2O 145 mg(0.5 mmol), phen 99 mg(0.5 mmol) 和L-丙氨酸89.1 mg(1 mmol),攪拌均勻后置恒溫箱中于120 ℃反應(yīng)3 d。自然冷卻至室溫,過(guò)濾,濾餅干燥得紅色塊狀晶體1,產(chǎn)率37%(以Co計(jì)算); IRν: 3 431, 3 224, 3 097, 1 651, 1 521, 1 431, 1 384, 1 284, 1 227, 1 151, 1 116, 1 036, 849, 720 cm-1; Anal.calcd for C18H26N5O11Co: C 40.13, H 5.27, N 12.98; found C 39.3, H 5.10, N 12.74 。
將1單晶(0.33 nm×0.26 nm×0.20 nm)置衍射儀上,以石墨單色化的鉬靶(λ=0.071 075 nm)輻射為光源,收集衍射數(shù)據(jù)。對(duì)所有數(shù)據(jù)進(jìn)行半經(jīng)驗(yàn)吸收校正,晶體結(jié)構(gòu)采用SHELXL-97程序[9]解析,采用理論計(jì)算方法對(duì)氫原子和非氫原子的各向同性和各向異性溫度因子進(jìn)行全矩陣最小二乘法修正。1的晶體學(xué)數(shù)據(jù)見(jiàn)表1。
表 1 1的晶體學(xué)參數(shù)Table 1 Crystal data and refinement details of 1
1的主要鍵長(zhǎng)和鍵角見(jiàn)表2,氫鍵鍵長(zhǎng)和鍵角見(jiàn)表3。圖1和圖2分別為1的分子結(jié)構(gòu)圖和三維結(jié)構(gòu)圖。
表 2 1的部分鍵長(zhǎng)和鍵角Table 2 Selection bond lengths and angles of 1
表 3 1的氫鍵鍵長(zhǎng)和鍵角Table 3 Hydrogen bond lengths and bond angles of 1
#1-x, -y+1 ,-z+1;#2-x+1, -y+1, -z+2;#3x, y-1, z
圖 1 1的分子結(jié)構(gòu)圖Figure 1 Molecular structure of 1
圖 2 1的三維氫鍵結(jié)構(gòu)圖Figure 2 3D structure of 1 formed by hydrogen bonds
圖3是1的熱分析曲線。由圖3可見(jiàn),1在63 ℃~270 ℃失重,分別于135 ℃和225 ℃出現(xiàn)兩個(gè)強(qiáng)的放熱峰,失重率約44%,對(duì)應(yīng)所失四個(gè)水分子和一個(gè)phen(理論值45.9%)。
Temperature/℃圖 3 1的熱分析曲線*Figure 3 Thermal analysis curves of 1*空氣氛,氣體流速60 mL·min-1,升溫速度15 ℃·min-1,掃描范圍0 ℃~400 ℃
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