Vibrational Dipole-Dipole Coupling and Long-Range Forces between Macromolecules

被引:1
|
作者
Sasihithlu, Karthik [1 ]
Scholes, Gregory D. [2 ]
机构
[1] Indian Inst Technol, Dept Energy Sci & Engn, Mumbai 400076, India
[2] Princeton Univ, Dept Chem, Princeton, NJ 08544 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2024年 / 128卷 / 05期
关键词
ENERGY-TRANSFER; EXCITATION TRANSFER; MOLECULAR MOBILITY;
D O I
10.1021/acs.jpcb.3c08251
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Long-range interactions between biomacromolecules are considered important for directing intracellular processes. Recent studies have posited that interactions between oscillating dipoles are well-suited to mediating long-range forces because they are weakly screened by a dielectric environment. Here, we extend these studies and present a quantum electrodynamic mechanism for resonant interactions between vibrational transition dipole moments of molecules. We explicitly consider the molecular charge density oscillations as IR transition dipoles. This gives a physical, molecular assignment to the idea of oscillating dipoles and allows us to develop explicit expressions for the interactions that can be quantified using parameters known from experiment. Moreover, in the same framework, we can describe van der Waals forces. We use numerical calculations to estimate the strength of resonant vibrational dipole-dipole interactions over long distances and compare these estimates to the van der Waals interaction. We find that the resonant vibrational dipole-dipole interactions dominate over the long range.
引用
收藏
页码:1205 / 1208
页数:4
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