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Synthesis of Conjugated Polymers from Surface Confined Highly Reactive Butadiyne Derivatives Tobe labratory Daichi Ando.

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Presentation on theme: "Synthesis of Conjugated Polymers from Surface Confined Highly Reactive Butadiyne Derivatives Tobe labratory Daichi Ando."— Presentation transcript:

1 Synthesis of Conjugated Polymers from Surface Confined Highly Reactive Butadiyne Derivatives Tobe labratory Daichi Ando

2 Introduction Topochemical Polymerization 10,12-Nonacosadiynoic acid Phthalocyanine STM Tip Okawa, Y.; Aono, M. J. Am. Chem. Soc. xxxx, xxx, 000-000.

3 Contents ・ STM ( Scanning Tunneling Microscope ) ・ Self-Assembly ・ Radical Polymerization ・ Background and Purpose of my project

4 STM Observations of Nanostructure Graphite Surface Au(111) Surface 1nm Ore of Gold (金の原石) Graphite STM PicoSTM (Agilent) Nanoscope IIIa (Digital Instruments) @Tobe lab.

5 5 Scanning Tunneling Microscopy (STM) e - V I d d I Quantum Tunneling d STM schematic diagram I = Ve -cd Tip Surface: Ag(111)

6 What’s Self - Assembly ? Water Droplets on Cold Glass Surface Product of Alum( ミョウバン ) DisorderOrder

7 Hydrogen bonding Self-Assembly van der Waals interaction 2D nano-architectures are constructed by molecular self-assembly. Heckl, W. M. et al. Single Mol. 2002, 3, 25.Charra, F. et al. Nano Lett. 2006, 6, 1360.

8 Hydrogen bond 8 Intermolecular interaction -Hydrogen bond- Lackinger, M.; Griessl, S.; Heckl, W. M.; Hietschold, M.; Flynn, G. W.; Langmuir, 2005, 21, 4984. Honeycomb( 蜂の巣 )

9 Intermolecular interaction -Van der Waals interaction- Van der waals interaction Bléger, D.; Kreher, D.; Mathevet, F.; Attias, A.-J.; Schull, G.; Huard, A.; Douillard, L.; Fiorini-Debuischert, C.; Charra, F. Angew. Chem. Int. Ed. 2007, 46, 7404–7407. 9

10 Homlytic Cleavage ( ホモリシス開裂 ) Radical Polymerization ( ラジカル重合 ) Radical Radical Polymerization Radical Stylene

11 Topochemical Polymerization of Butadiyne Derivatives on Surface Okawa, Y.; Aono, M. J. Chem. Phys. 2001, 115, 2317-2322. Monomer molecule Chain propagation

12 Previous Research Octaehydrobenzo[12]annulene Derivatives Polymerization Octadehydrobenzo[12]annulene (DBA) Tobe, Y. et al. Chem. Eur. J. 2010, 16, 8319-8328. 5.9 – 6.1 nm

13 Purpose of This work external stimuliPolymerization Polyacene Radical Intermediate Previous SubjectFollowing Subject

14

15 SnowflakeFeather of Peafowl Zebra’s pattern Heartbeat What’s Self - Assembly ?

16 Topochemical Polymerization of Butadiyne Derivatives on Surface Okawa, Y.; Aono, M. J. Chem. Phys. 2001, 115, 2317-2322. Monomer molecule h Electronic excitation Vibration excitation Addition reaction Chain propagation

17 Dehydrobenzo[12]annulene Derivatives Zhou, Q.; Carrol, P. J.; Swager, T. M. J. Org. Chem. 1994, 59, 1294-1301. 1a: R = C 10 H 21 1b: R = OC 12 H 25 1c: R = OC 14 H 29 1d: R = OC 16 H 33 1e: R = OC 18 H 37 1f: R = OC 20 H 41 Polymerization Octadehydrobenzo[12]annulene (DBA) 1 1a Tobe, Y. et al. Chem. Eur. J. 2010, 16, 8319-8328. 5.9 – 6.1 nm

18 h or pulse voltage


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