Radiation Laboratory and Department of Physics, University of Notre Dame, Notre Dame, Indiana 46556, USA.
J Chem Phys. 2011 Dec 7;135(21):214309. doi: 10.1063/1.3664784.
Gas phase studies of dissociative electron attachment to simple alkyl (CF(3)SO(3)CH(3)) and aryl (C(6)H(5)SO(3)CF(3) and CF(3)SO(3)C(6)H(4)CH(3)) triflates, model molecules of nonionic photoacid generators for modern lithographic applications, were performed. The fragmentation pathways under electron impact below 10 eV were identified by means of crossed electron-molecular beam mass spectrometry. Major dissociation channels involved C-O, S-O, or C-S bond scissions in the triflate moiety leading to the formation of triflate (OTf(-)), triflyl (Tf(-)), or sulfonate (RSO(3)(-)) anions, respectively. A resonance leading to C-O bond breakage and OTf(-) formation in alkyl triflates occurred at electron energies about 0.5 eV lower than the corresponding resonance in aryl triflates. A resonance leading to S-O bond breakage and Tf(-) formation in aryl triflates occurred surprisingly at the same electron energies as C-O bond breakage. In case of alkyl triflates S-O bond breakage required 1.4 eV higher electron energies to occur and proceeded with substantially lower yields than in aryl triflates. C-S bond scission occurred for all presently studied triflates at energies close to 3 eV.
气相中研究简单的烷基(CF(3)SO(3)CH(3))和芳基(C(6)H(5)SO(3)CF(3)和 CF(3)SO(3)C(6)H(4)CH(3))三氟甲磺酸酯的电子的亲核反应,作为现代光刻应用的非离子光酸产生剂的模型分子,被进行了。在 10 电子伏特以下的电子冲击下,通过交叉电子-分子束质谱法确定了碎片途径。主要的解离通道涉及三氟甲磺酸酯部分的 C-O、S-O 或 C-S 键断裂,分别导致形成三氟甲磺酸根(OTf(-))、三氟甲基(Tf(-))或磺酸盐(RSO(3)(-))阴离子。在烷基三氟甲磺酸酯中,导致 C-O 键断裂和 OTf(-)形成的共振出现在比芳基三氟甲磺酸酯中相应的共振低约 0.5 电子伏特的电子能量处。在芳基三氟甲磺酸酯中,导致 S-O 键断裂和 Tf(-)形成的共振出人意料地出现在与 C-O 键断裂相同的电子能量处。对于烷基三氟甲磺酸酯,S-O 键断裂需要 1.4 电子伏特更高的电子能量才能发生,并且产率远低于芳基三氟甲磺酸酯。所有目前研究的三氟甲磺酸酯在接近 3 电子伏特的能量下发生 C-S 键断裂。