1,3-dipolar cycloaddition for the generation of nanostructured semiconductors by heated probe tips

被引:87
作者
Bakbak, Selma
Leech, Peter J.
Carson, Bradley E.
Saxena, Shubham
King, William P. [1 ]
Bunz, Uwe H. F.
机构
[1] Georgia Inst Technol, George W Woodruff Sch Mech Engn, Atlanta, GA 30332 USA
[2] Georgia Inst Technol, Sch Chem & Biochem, Atlanta, GA 30332 USA
关键词
D O I
10.1021/ma0615912
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The 1,3-Dipolar cycloadditions of terminal diynes with aromatic diazides are used for the generation of nanostructured organic semiconductors by heated atomic force microscope (AFM) cantilever tips. The fabrication is done by nanoscale thermal processing of annealed diazide/dialkyne thin films. The cantilever tip was brought into contact with the film with a load force of ~100 nN and heated. Precision calibration of the cantilever was possible and the tip temperature was near 225 °C. Conjugated polymer form from azide and alkyne precursors under thermal and Cu-catalyzed conditions. It is possible to write crisp nanoscale features into mixed diazide-diyne films after preannealing, using a heated cantilever. The absence of thickness and ripping makes this materials particularly attractive as novel organic semiconductors that can be easily thermally structured.
引用
收藏
页码:6793 / 6795
页数:3
相关论文
共 39 条
[1]   Conducting polymers in microelectronics [J].
Angelopoulos, M .
IBM JOURNAL OF RESEARCH AND DEVELOPMENT, 2001, 45 (01) :57-75
[2]   Combining ring-opening metathesis polymerization (ROMP) with sharpless-type "click" reactions: An easy method for the preparation of side chain functionalized poly(oxynorbornenes) [J].
Binder, WH ;
Kluger, C .
MACROMOLECULES, 2004, 37 (25) :9321-9330
[3]   Organic azides:: An exploding diversity of a unique class of compounds [J].
Bräse, S ;
Gil, C ;
Knepper, K ;
Zimmermann, V .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2005, 44 (33) :5188-5240
[4]  
BUNZ UH, 2000, ADV MATER, V18, P973
[5]   Synthesis and structure of PAEs [J].
Bunz, UHF .
POLY(ARYLENE ETYNYLENE)S: FROM SYNTHESIS TO APPLICATION, 2005, 177 :1-52
[6]   Poly(aryleneethynylene)s: Syntheses, properties, structures, and applications [J].
Bunz, UHF .
CHEMICAL REVIEWS, 2000, 100 (04) :1605-1644
[7]   Self-assembly of conjugated molecular rods: A high-resolution STM study [J].
Dhirani, AA ;
Zehner, RW ;
Hsung, RP ;
GuyotSionnest, P ;
Sita, LR .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1996, 118 (13) :3319-3320
[8]   Fabrication of polypyrrole wires between microelectrodes [J].
Dong, B ;
Krutschke, M ;
Zhang, X ;
Chi, LF ;
Fuchs, H .
SMALL, 2005, 1 (05) :520-524
[9]   Click chemistry as a powerful tool for the construction of functional poly(p-phenyleneethynylene)s:: Comparison of pre- and postfunctionalization schemes [J].
Englert, BC ;
Bakbak, S ;
Bunz, UHF .
MACROMOLECULES, 2005, 38 (14) :5868-5877
[10]   Dendronized linear polymers via "click chemistry" [J].
Helms, B ;
Mynar, JL ;
Hawker, CJ ;
Fréchet, JMJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (46) :15020-15021