Long-Range Chirality Recognition of a Polar Molecule on Au(111)

被引:18
作者
Kong, Huihui [1 ]
Qian, Yinyue [1 ]
Liu, Xinbang [1 ]
Wan, Xinling [1 ]
Amirjalayer, Saeed [2 ,3 ,4 ]
Fuchs, Harald [1 ,2 ,3 ]
机构
[1] Nanjing Univ Sci & Technol, Herbert Gleiter Inst Nanosci, Sch Mat Sci & Engn, Nanjing 210094, Jiangsu, Peoples R China
[2] Westfalische Wilhelms Univ Munster, Phys Inst, D-48149 Munster, Germany
[3] Ctr Nanotechnol CeNTech, Heisenbergstr 11, D-48149 Munster, Germany
[4] CMTC, Heisenbergstr 11, D-48149 Munster, Germany
基金
中国国家自然科学基金;
关键词
Au(111); density functional calculations; dipoles; long-range chirality recognition; scanning tunneling microscopy; CLUSTERS; ADSORPTION; COMPLEXES; SURFACE;
D O I
10.1002/anie.201909593
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chiral molecular self-assemblies were usually achieved using short-range intermolecular interactions, such as hydrogen-, metal-organic, and covalent bonding. However, unavoidable surface defects, such as step edges, surface reconstructions, or site dislocations may limit the applicability of short-range chirality recognition. Long-range chirality recognition on surfaces would be an appealing but challenging strategy for chiral reservation across surface defects at long distances. Now, long-range chirality recognition is presented between neighboring 3-bromo-naphthalen-2-ol (BNOL) stripes on an inert Au(111) surface across the herringbone reconstruction as investigated by STM and DFT calculations. The key to achieving such recognition is the herringbone reconstruction-induced local dipole accumulation at the edges of the BNOL stripes. The neighboring stripes are then forced to adopt the same chirality to create the opposite edged dipoles and neutralize the neighbored dipole moments.
引用
收藏
页码:182 / 186
页数:5
相关论文
共 37 条
[1]   Stereoselectivity and electrostatics in charge-transfer Mn- and Cs-TCNQ4 networks on Ag(100) [J].
Abdurakhmanova, Nasiba ;
Floris, Andrea ;
Tseng, Tzu-Chun ;
Comisso, Alessio ;
Stepanow, Sebastian ;
De Vita, Alessandro ;
Kern, Klaus .
NATURE COMMUNICATIONS, 2012, 3
[2]  
[Anonymous], 2006, Angew. Chem
[3]   Chiral salen complexes: An overview to recoverable and reusable homogeneous and heterogeneous catalysts [J].
Baleizao, Carlos ;
Garcia, Hermenegildo .
CHEMICAL REVIEWS, 2006, 106 (09) :3987-4043
[4]   Long-range chiral recognition due to substrate locking and substrate-adsorbate charge transfer [J].
Blankenburg, S. ;
Schmidt, W. G. .
PHYSICAL REVIEW LETTERS, 2007, 99 (19)
[5]   ENANTIOSELECTIVE SYNTHESIS USING CHIRAL HETEROGENEOUS CATALYSTS [J].
BLASER, HU .
TETRAHEDRON-ASYMMETRY, 1991, 2 (09) :843-866
[6]  
Blum M.-C., 2005, ANGEW CHEM, V117, P5468
[7]   Conservation of chirality in a hierarchical supramolecular self-assembled structure with pentagonal symmetry [J].
Blüm, MC ;
Cavar, E ;
Pivetta, M ;
Patthey, F ;
Schneider, WD .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (33) :5334-5337
[8]  
Böhringer M, 1999, ANGEW CHEM INT EDIT, V38, P821, DOI 10.1002/(SICI)1521-3773(19990315)38:6<821::AID-ANIE821>3.0.CO
[9]  
2-A
[10]   Two-dimensional self-assembly of supramolecular clusters and chains [J].
Böhringer, M ;
Morgenstern, K ;
Schneider, WD ;
Berndt, R ;
Mauri, F ;
De Vita, A ;
Car, R .
PHYSICAL REVIEW LETTERS, 1999, 83 (02) :324-327