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巴基二茂铁的双自由基特性及非线性光学性质:聚焦于适当修饰的富勒烯片段的应用

Diradical character and nonlinear optical properties of buckyferrocenes: focusing on the use of suitably modified fullerene fragments.

作者信息

Muhammad Shabbir, Ito Soichi, Nakano Masayoshi, Kishi Ryohei, Yoneda Kyohei, Kitagawa Yasutaka, Shkir Mohd, Irfan Ahmad, Chaudhry Aijaz R, AlFaify Salem, Kalam Abul, Al-Sehemi Abdullah G

机构信息

Department of Physics, College of Science, King Khalid University, Abha 61413, P.O. Box 9004, Saudi Arabia.

出版信息

Phys Chem Chem Phys. 2015 Feb 28;17(8):5805-16. doi: 10.1039/c4cp05175k.

Abstract

The buckyferrocenes, synthesized through face-to-face fusion of ferrocene and fullerene fragments (C60Me10), are expected to enjoy the rich scientific heritage of ferrocene and fullerene with an extensively large π-conjugation network between the two Fe atoms [Y. Matsuo, K. Tahara and E. Nakamura, J. Am. Chem. Soc., 2006, 128, 7154]. However, the addition of pentamethyl groups at each end of the fullerene fragment breaks the π-conjugation path as well as metal-metal spin correlation between the two-ferrocene faces in a buckyferrocene. We found that the unblocking of π-conjugation from different positions in fullerene fragments have substantial effects on their topologies, spin densities, diradical characters as well as nonlinear optical (NLO) properties of these buckyferrocenes. We study the topological dependence of open-shell diradical character and second hyperpolarizability (γ), the third-order NLO properties at the molecular scale, in several buckyferrocenes. On the basis of their different diradical characters (yi), which are defined by the occupation number of the lowest unoccupied natural orbital (LUNO) + i (i = 0, 1,…), these buckyferrocenes are categorized into three groups, i.e., closed-shell (yi = 0), intermediate open-shell singlet (0 < yi < 1), and almost pure open-shell singlet (yi = 1) compounds. For example, we found that buckyferrocenes including (CpFe)2η(5)C60Me10 and (CpFe)2η(5)C70Me10 have closed-shell configurations. The buckyferrocenes (CpFe)2η(5)C60, (CpFe)2η(5)C70, (CpFe)2η(5)C70Me8, (CpFe)2η(5)C70Me4 and (CpFe)2η(5)C30 are intermediate open-shell singlet, while (CpFe)2η(5)C60Me4 and (CpFe)2η(5)C60Me8 are pure open-shell singlet complexes. Interestingly, the γzzzz amplitude of (CpFe)2η(5)C60, an open-shell intermediate diradical complex, is about 41 times and 13 times as large as those of its closed-shell ((CpFe)2η(5)C60Me10) and pure diradical ((CpFe)2η(5)C60Me8) counterparts, respectively. Similarly, the γzzzz amplitudes of (CpFe)2η(5)C70, (CpFe)2η(5)C70Me4, and (CpFe)2η(5)C70Me8 with intermediate diradical character are about 36, 17, and 9 times as large as that of their closed-shell (CpFe)2η(5)C70Me10 counterpart. The fact that larger γzzzz values are obtained for buckyferrocenes with intermediate diradical characters is in line with the "y-γ correlation" obtained from the valence configuration interaction (VCI) results for a two-site diradical model [M. Nakano, et al., Phys. Rev. Lett., 2007, 99, 033001] as well as for fullerene and graphene systems. The γzzzz density analysis shows that the large positive contributions originate from the large γzzzz density distributions on the upper- and lower-extended edges of the buckyferrocenes, between which significant spin polarizations appear within the spin-unrestricted DFT level of theory. These results demonstrate that such buckyferrocenes are potential candidates for a novel class of open-shell singlet NLO systems, where γzzzz values are modulated by tuning their diradical character through the use of suitably modified fullerene fragments.

摘要

通过二茂铁和富勒烯片段(C60Me10)面对面融合合成的巴基二茂铁,有望继承二茂铁和富勒烯丰富的科学遗产,且两个铁原子之间具有广泛的大π共轭网络[松尾洋、田原健和中村英夫,《美国化学会志》,2006年,128卷,7154页]。然而,在富勒烯片段的两端各添加五个甲基,会破坏π共轭路径以及巴基二茂铁中两个二茂铁面之间的金属 - 金属自旋相关性。我们发现,从富勒烯片段的不同位置解除π共轭封锁,对这些巴基二茂铁的拓扑结构、自旋密度、双自由基特性以及非线性光学(NLO)性质都有显著影响。我们研究了几种巴基二茂铁在分子尺度上开壳双自由基特性和二阶超极化率(γ)(三阶NLO性质)的拓扑依赖性。基于它们不同的双自由基特性(yi),这些特性由最低未占据自然轨道(LUNO) + i(i = 0, 1, …)的占据数定义,这些巴基二茂铁被分为三组,即闭壳(yi = 0)、中间开壳单重态(0 < yi < 1)和几乎纯的开壳单重态(yi = 1)化合物。例如,我们发现包含(CpFe)2η(5)C60Me10和(CpFe)2η(5)C70Me10的巴基二茂铁具有闭壳构型。巴基二茂铁(CpFe)2η(5)C60、(CpFe)2η(5)C70、(CpFe)2η(5)C70Me8、(CpFe)2η(5)C70Me4和(CpFe)2η(5)C30是中间开壳单重态,而(CpFe)2η(5)C60Me4和(CpFe)2η(5)C60Me8是纯开壳单重态配合物。有趣的是,开壳中间双自由基配合物(CpFe)2η(5)C60的γzzzz振幅分别约为其闭壳对应物((CpFe)2η(5)C60Me10)和纯双自由基对应物((CpFe)2η(5)C60Me8)的41倍和13倍。同样,具有中间双自由基特性的(CpFe)2η(5)C70、(CpFe)2η(5)C70Me4和(CpFe)2η(5)C70Me8的γzzzz振幅分别约为其闭壳对应物(CpFe)2η(5)C70Me10的36倍、17倍和9倍。对于具有中间双自由基特性的巴基二茂铁获得更大的γzzzz值这一事实,与从双位点双自由基模型的价电子构型相互作用(VCI)结果[中野猛,等人,《物理评论快报》,2007年,99卷,033001]以及富勒烯和石墨烯系统中得到的“y - γ相关性”一致。γzzzz密度分析表明,大的正贡献源于巴基二茂铁上下延伸边缘上大的γzzzz密度分布,在自旋非限制密度泛函理论水平下,两者之间出现了显著的自旋极化。这些结果表明,此类巴基二茂铁是新型开壳单重态NLO系统的潜在候选者,其中γzzzz值可通过使用适当修饰的富勒烯片段调节其双自由基特性来调控。

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