Tang Huadong, Arulsamy Navamoney, Radosz Maciej, Shen Youqing, Tsarevsky Nicolay V, Braunecker Wade A, Tang Wei, Matyjaszewski Krzysztof
Soft Materials Laboratory, Department of Chemical & Petroleum Engineering, University of Wyoming, Laramie, Wyoming 82071, USA.
J Am Chem Soc. 2006 Dec 20;128(50):16277-85. doi: 10.1021/ja0653369.
Atom transfer radical polymerization (ATRP) generally requires a catalyst/initiator molar ratio of 0.1 to 1 and catalyst/monomer molar ratio of 0.001 to 0.01 (i.e., catalyst concentration: 1000-10,000 ppm versus monomer). Herein, we report a new copper-based complex CuBr/N,N,N',N'-tetrakis(2-pyridylmethyl)ethylenediamine (TPEN) as a versatile and highly active catalyst for acrylic, methacrylic, and styrenic monomers. The catalyst mediated ATRP at a catalyst/initiator molar ratio of 0.005 and produced polymers with well-controlled molecular weights and low polydispersities. ATRP occurred even at a catalyst/initiator molar ratio as low as 0.001 with copper concentration in the produced polymers as low as 6-8 ppm (catalyst/monomer molar ratio = 10(-5)). The catalyst structures were studied by X-ray diffraction and NMR spectroscopy. The activator CuIBr/TPEN existed in solution as binuclear and mononuclear complexes in equilibrium but as a binuclear complex in its single crystals. The deactivator CuIIBr2/TPEN complex was mononuclear. High stability and appropriate KATRP (ATRP equilibrium constant) were found crucial for the catalyst working under high dilution or in coordinating solvents/monomers. This provides guidance for further design of highly active ATRP catalysts.
原子转移自由基聚合(ATRP)通常需要催化剂/引发剂的摩尔比为0.1至1,以及催化剂/单体的摩尔比为0.001至0.01(即催化剂浓度:相对于单体为1000 - 10,000 ppm)。在此,我们报道了一种新型的铜基配合物CuBr/N,N,N',N'-四(2-吡啶甲基)乙二胺(TPEN),它是用于丙烯酸、甲基丙烯酸和苯乙烯类单体的通用且高活性催化剂。该催化剂在催化剂/引发剂摩尔比为0.005时介导ATRP反应,并生成分子量可控且多分散性低的聚合物。即使在催化剂/引发剂摩尔比低至0.001时,ATRP反应仍能发生,所生成聚合物中的铜浓度低至6 - 8 ppm(催化剂/单体摩尔比 = 10⁻⁵)。通过X射线衍射和核磁共振光谱对催化剂结构进行了研究。活化剂CuIBr/TPEN在溶液中以双核和单核配合物的平衡形式存在,但在其单晶中为双核配合物。失活剂CuIIBr2/TPEN配合物为单核。发现高稳定性和合适的KATRP(ATRP平衡常数)对于催化剂在高稀释条件下或在配位溶剂/单体中发挥作用至关重要。这为进一步设计高活性ATRP催化剂提供了指导。