Interactive Chemical Reactivity Exploration

被引:51
作者
Haag, Moritz P. [1 ]
Vaucher, Alain C. [1 ]
Bosson, Mael [2 ,3 ]
Redon, Stephane [2 ,3 ]
Reiher, Markus [1 ]
机构
[1] ETH, Lab Phys Chem, CH-8093 Zurich, Switzerland
[2] INRIA Grenoble Rhone Alpes, NANO D, F-38334 Saint Ismier, France
[3] CNRS, Lab Jean Kuntzmann, F-38334 Saint Ismier, France
基金
欧洲研究理事会;
关键词
chemical reactivity; haptic quantum chemistry; interactive quantum chemistry; potential energy surfaces; real-time quantum chemistry; ELECTRONIC-STRUCTURE CALCULATIONS; DENSITY-FUNCTIONAL THEORY; GENERATION; CHARGE; CONSTRUCTION; SIMULATIONS; MECHANISMS; DYNAMICS; VALENCE; COMPLEX;
D O I
10.1002/cphc.201402342
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
Elucidating chemical reactivity in complex molecular assemblies of a few hundred atoms is, despite the remarkable progress in quantum chemistry, still a major challenge. Black-box search methods to find intermediates and transition-state structures might fail in such situations because of the high-dimensionality of the potential energy surface. Here, we propose the concept of interactive chemical reactivity exploration to effectively introduce the chemist's intuition into the search process. We employ a haptic pointer device with force feedback to allow the operator the direct manipulation of structures in three dimensions along with simultaneous perception of the quantum mechanical response upon structure modification as forces. We elaborate on the details of how such an interactive exploration should proceed and which technical difficulties need to be overcome. All reactivity-exploration concepts developed for this purpose have been implemented in the samson programming environment.
引用
收藏
页码:3301 / 3319
页数:19
相关论文
共 76 条
  • [1] ELECTRONIC-STRUCTURE CALCULATIONS ON WORKSTATION COMPUTERS - THE PROGRAM SYSTEM TURBOMOLE
    AHLRICHS, R
    BAR, M
    HASER, M
    HORN, H
    KOLMEL, C
    [J]. CHEMICAL PHYSICS LETTERS, 1989, 162 (03) : 165 - 169
  • [2] ELECTRON-DENSITY DISTRIBUTION-FUNCTIONS AND THE ASED-MO THEORY
    ANDERSON, AB
    [J]. INTERNATIONAL JOURNAL OF QUANTUM CHEMISTRY, 1994, 49 (05) : 581 - 589
  • [3] DFTB+, a sparse matrix-based implementation of the DFTB method
    Aradi, B.
    Hourahine, B.
    Frauenheim, Th.
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 2007, 111 (26) : 5678 - 5684
  • [4] POSTULATED ELECTROCYCLIC REACTIONS LEADING TO ENDIANDRIC ACID AND RELATED NATURAL-PRODUCTS
    BANDARANAYAKE, WM
    BANFIELD, JE
    BLACK, DSC
    [J]. JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1980, (19) : 902 - 903
  • [5] DENSITY-FUNCTIONAL THERMOCHEMISTRY .3. THE ROLE OF EXACT EXCHANGE
    BECKE, AD
    [J]. JOURNAL OF CHEMICAL PHYSICS, 1993, 98 (07) : 5648 - 5652
  • [6] Bergeler M., UNPUB
  • [7] Bolopion A., WORLD HAPT C WHC 201, P469
  • [8] Comparing position and force control for interactive molecular simulators with haptic feedback
    Bolopion, Aude
    Cagneau, Barthelemy
    Redon, Stephane
    Regnier, Stephane
    [J]. JOURNAL OF MOLECULAR GRAPHICS & MODELLING, 2010, 29 (02) : 280 - 289
  • [9] Interactive quantum chemistry: A divide-and-conquer ASED-MO method
    Bosson, Maeel
    Richard, Caroline
    Plet, Antoine
    Grudinin, Sergei
    Redon, Stephane
    [J]. JOURNAL OF COMPUTATIONAL CHEMISTRY, 2012, 33 (07) : 779 - 790
  • [10] Block-adaptive quantum mechanics: An adaptive divide-and-conquer approach to interactive quantum chemistry
    Bosson, Mael
    Grudinin, Sergei
    Redon, Stephane
    [J]. JOURNAL OF COMPUTATIONAL CHEMISTRY, 2013, 34 (06) : 492 - 504