Facultad de Física, Pontificia Universidad Católica de Chile, Santiago 22, Chile.
J Chem Phys. 2009 Sep 21;131(11):114705. doi: 10.1063/1.3213642.
Crystalline-to-rotator phase transitions have been widely studied in bulk hydrocarbons, in particular in normal alkanes. But few studies of these transitions deal with molecularly thin films of pure n-alkanes on solid substrates. In this work, we were able to grow dotriacontane (n-C(32)H(66)) films without coexisting bulk particles, which allows us to isolate the contribution to the ellipsometric signal from a monolayer of molecules oriented with their long axis perpendicular to the SiO(2) surface. For these submonolayer films, we found a step in the ellipsometer signal at approximately 331 K, which we identify with a solid-solid phase transition. At higher coverages, we observed additional steps in the ellipsometric signal that we identify with a solid-solid phase transition in multilayer islands ( approximately 333 K) and with the transition to the rotator phase in bulk crystallites ( approximately 337 K), respectively. After considering three alternative explanations, we propose that the step upward in the ellipsometric signal observed at approximately 331 K on heating the submonolayer film is the signature of a transition from a perpendicular monolayer phase to a denser phase in which the alkane chains contain on average one to two gauche defects per molecule.
晶体-旋转相转变在大块碳氢化合物中,特别是在正构烷烃中得到了广泛的研究。但是,很少有研究涉及到纯正构烷烃在固体基底上的分子层薄。在这项工作中,我们成功地生长了没有共存体相颗粒的三十二烷(n-C(32)H(66))薄膜,这使得我们能够从与 SiO(2)表面垂直取向的单层分子中分离出椭圆偏振信号的贡献。对于这些亚单层薄膜,我们在大约 331 K 时发现椭圆偏振信号中的一个阶跃,我们将其识别为固态-固态相变。在更高的覆盖率下,我们观察到椭圆偏振信号中的附加阶跃,我们将其分别识别为多层岛中的固态-固态相变(大约 333 K)和晶相中旋转相的转变(大约 337 K)。在考虑了三种替代解释之后,我们提出在亚单层薄膜加热时,在大约 331 K 观察到的椭圆偏振信号向上的阶跃是从垂直单层相到密度更大的相的转变的特征,其中烷烃链平均每个分子含有一个到两个 gauche 缺陷。