Sun F X,Zhu G S. Solvent-directed synthesis of chiral and non-centrosymmetric metal-organic frameworks based on pyridine-3,5-dicarboxylate[J]. Inorg. Chem. Commun.,2013,38:115-18.
[2]
Kepert C J,Prior T J,Rosseinsky M J. A versatile family of interconvertible microporous chiral molecular frameworks:The first example of ligand control of network chirality[J]. J. Am. Chem. Soc.,2000,122(21):5158-5168.
[3]
Bradshaw D,Prior T J,Cussen E J,et al. Permanent microporosity and enantioselective sorption in a chiral open framework[J]. J. Am. Chem. Soc.,2004,126(19):6106-6114.
Lin Z J,Slawin A M Z,Morris R E. Chiral induction in the ionothermal synthesis of a coordination polymer[J]. J. Am. Chem. Soc.,2007,129(16):4880-4881.
[10]
李宁. 田口设计方法在科研院所应用研究[J]. 电子质量,2011,8:1-2,22.
[11]
Liang L L,Ren S B,Zhang J,et al. Two thermostable three-dimensional homochiral metal-organic polymers with quartz topology[J]. Cryst. Growth Des.,2010,10(3):1307-1311.
[12]
Khazini L. Fatehifar E,Fouladpanjeh B. Application of the Taguchi method for the optimization of an amine-based tail gas treating unit in petroleum refineries[J]. Energy Sources Part A-Recovery Utilization and Environmental Effects,2014,36(7):709-718.
[13]
Zhang J,Yao Y G,Bu X H. Comparative study of homochiral and racemic chiral metal-organic frameworks built from camphoric acid[J]. Chem. Mater.,2007,19(21):5083-5089.
Ingleson M J,Barrio J P,Bacsa J,et al. Generation of a solid Br？sted acid site in a chiral framework[J]. Chem. Commun.,2008,11:1287-1289.
[17]
Chuang Ho-Chiao,Lee Wen-Fu. Parametric optimization of Nd-YVO4 laser for straight scribing on silver nanowire based conductive thin films by Taguchi method[J]. Optics and Laser Technology,2014,57(s1):149-153.
[18]
洪楠,侯军. Minitab统计分析教程[M]. 北京:电子工业出版社,2007.
[19]
Cho S H,Ma B Q,Nguyen S T,et al. A metal-organic framework material that functions as an enantioselective catalyst for olefin epoxidation[J]. Chem. Commun.,2006,2563-2565.
