O'Mullane Anthony P, Fay Nigel, Nafady Ayman, Bond Alan M
School of Chemistry, Monash University, Clayton, Victoria 3800, Australia.
J Am Chem Soc. 2007 Feb 21;129(7):2066-73. doi: 10.1021/ja066874o. Epub 2007 Jan 27.
A generic method for the synthesis of metal-7,7,8,8-tetracyanoquinodimethane (TCNQ) charge-transfer complexes on both conducting and nonconducting substrates is achieved by photoexcitation of TCNQ in acetonitrile in the presence of a sacrificial electron donor and the relevant metal cation. The photochemical reaction leads to reduction of TCNQ to the TCNQ(-) monoanion. In the presence of M(x+)(MeCN), reaction with TCNQ(-)(MeCN) leads to deposition of M(x+)[TCNQ]x crystals onto a solid substrate with morphologies that are dependent on the metal cation. Thus, CuTCNQ phase I photocrystallizes as uniform microrods, KTCNQ as microrods with a random size distribution, AgTCNQ as very long nanowires up to 30 mum in length and with diameters of less than 180 nm, and CoTCNQ(H(2)O)(2) as nanorods and wires. The described charge-transfer complexes have been characterized by optical and scanning electron microscopy and IR and Raman spectroscopy. The CuTCNQ and AgTCNQ complexes are of particular interest for use in memory storage and switching devices. In principle, this simple technique can be employed to generate all classes of metal-TCNQ complexes and opens up the possibility to pattern them in a controlled manner on any type of substrate.
一种在导电和非导电基底上合成金属 - 7,7,8,8 - 四氰基对苯二醌二甲烷(TCNQ)电荷转移配合物的通用方法,是通过在牺牲电子供体和相关金属阳离子存在下,在乙腈中对TCNQ进行光激发来实现的。光化学反应导致TCNQ还原为TCNQ(-)单阴离子。在M(x +)(MeCN)存在下,与TCNQ(-)(MeCN)反应会导致M(x +)[TCNQ]x晶体沉积在固体基底上,其形态取决于金属阳离子。因此,CuTCNQ第一相光结晶为均匀的微棒,KTCNQ为尺寸分布随机的微棒,AgTCNQ为长度达30μm且直径小于180nm的非常长的纳米线,而CoTCNQ(H(2)O)(2)为纳米棒和纳米线。所描述的电荷转移配合物已通过光学和扫描电子显微镜以及红外和拉曼光谱进行了表征。CuTCNQ和AgTCNQ配合物在用于存储和开关器件方面特别受关注。原则上,这种简单技术可用于生成所有类型的金属 - TCNQ配合物,并开辟了以可控方式在任何类型基底上对其进行图案化的可能性。