Enabling Rapid and Accurate Construction of CCSD(T)-Level Potential Energy Surface of Large Molecules Using Molecular Tailoring Approach

鞍点 势能面 乙酰丙酮 工作(物理) 分子 基态 势能 原子物理学 最大值和最小值 化学 计算化学 材料科学 物理 热力学 量子力学 几何学 数学 数学分析 无机化学
作者
Subodh S. Khire,Nalini D. Gurav,Apurba Nandi,Shridhar R. Gadre
出处
期刊:Journal of Physical Chemistry A [American Chemical Society]
卷期号:126 (8): 1458-1464 被引量:7
标识
DOI:10.1021/acs.jpca.2c00025
摘要

The construction of a potential energy surface (PES) of even a medium-sized molecule employing correlated theory, such as CCSD(T), is arduous due to the high computational cost involved. The present study reports the possibility of efficiently constructing such a PES of molecules containing up to 15 atoms and 550 basis functions by employing the fragment-based molecular tailoring approach (MTA) on off-the-shelf hardware. The MTA energies at the CCSD(T)/aug-cc-pVTZ level for several geometries of three test molecules, viz., acetylacetone, N-methylacetamide, and tropolone, are reported. These energies are in excellent agreement with their full calculation counterparts with a time advantage factor of 3-5. The energy barrier from the ground to transition state is also accurately captured. Further, we demonstrate the accuracy and efficiency of MTA for estimating the energy gradients at the CCSD(T) level. As a further application of our MTA methodology, the energies of acetylacetone at ∼430 geometries are computed at the CCSD(T)/aug-cc-pVTZ level and used for generating a Δ-machine learning (Δ-ML) PES. This leads to the H-transfer barrier of 3.02 kcal/mol, well in agreement with the benchmarked barrier of 3.19 kcal/mol. The fidelity of this Δ-ML PES is examined by geometry optimization and normal mode frequency calculations of global minima and saddle point geometries. We trust that the present work is a major development for the rapid and accurate construction of PES at the CCSD(T) level for molecules containing up to 20 atoms and 600 basis functions using off-the-shelf hardware.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
华仔应助超级的眼睛采纳,获得10
刚刚
刚刚
拼搏太英发布了新的文献求助10
刚刚
1秒前
Jasper应助sscihard采纳,获得10
1秒前
Nn完成签到,获得积分20
1秒前
orixero应助水易而华采纳,获得10
1秒前
鸢尾完成签到,获得积分10
2秒前
领导范儿应助Randy采纳,获得10
2秒前
ixxxy完成签到,获得积分10
3秒前
sbxfly完成签到,获得积分10
3秒前
3秒前
领导范儿应助77888采纳,获得30
3秒前
张鱼大丸子完成签到,获得积分10
3秒前
罗先斗完成签到,获得积分10
4秒前
Nn发布了新的文献求助10
4秒前
余悸发布了新的文献求助10
4秒前
科研通AI6.1应助柒姐采纳,获得10
4秒前
内向初瑶完成签到,获得积分10
4秒前
科目三应助勤奋丝袜采纳,获得10
5秒前
所所应助终于花开日采纳,获得10
5秒前
liuyc完成签到 ,获得积分10
5秒前
木婉清发布了新的文献求助150
5秒前
6秒前
ccc发布了新的文献求助20
6秒前
gdgd发布了新的文献求助10
6秒前
寮信应助stevenli采纳,获得10
7秒前
Rita应助stevenli采纳,获得10
7秒前
所所应助瑞瑞1988采纳,获得10
7秒前
WW发布了新的文献求助10
7秒前
9秒前
FashionBoy应助JJJJJJJJJ采纳,获得10
10秒前
10秒前
yy完成签到 ,获得积分10
10秒前
10秒前
11秒前
JLY发布了新的文献求助10
12秒前
科目三应助dxzdxj采纳,获得10
13秒前
Verdurie应助dxzdxj采纳,获得20
13秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Developing Genetic Editing Tools for Lysobacter 2000
Моделирование процессов самоорганизации в кристаллообразующих системах 1000
History of U.S. Space Surveillance and Satellite Cataloging 1000
Adhesion Science: Principles & Practice 800
Signals, Systems, and Signal Processing 610
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 600
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6525445
求助须知:如何正确求助?哪些是违规求助? 8318718
关于积分的说明 17802770
捐赠科研通 5627006
什么是DOI,文献DOI怎么找? 2929177
邀请新用户注册赠送积分活动 1905915
关于科研通互助平台的介绍 1765647