عنوان

On-surface synthesis II :

(Number (ISBN

3319758101

(Number (ISBN

9783319758107

Erroneous ISBN

3319758098

Erroneous ISBN

9783319758091

Title Proper

On-surface synthesis II :

General Material Designation

[Book]

Other Title Information

proceedings of the International Workshop On-Surface Synthesis, San Sebastián, 27-30 June 2016 /

First Statement of Responsibility

Dimas G. de Oteyza, Celia Rogero, editors.

Place of Publication, Distribution, etc.

Cham, Switzerland :

Name of Publisher, Distributor, etc.

Springer,

Date of Publication, Distribution, etc.

2018.

Specific Material Designation and Extent of Item

1 online resource (viii, 227 pages)

Series Title

Advances in atom and single molecule machines,

ISSN of Series

2193-9691

Text of Note

Intro; Preface; Contents; 1 Mechanistic Insights into Surface-Supported Chemical Reactions; Abstract; 1 Introduction; 2 Imaging and Counting Intermediates; 3 Why Are Intermediates Stabilized?; 4 Bringing It All Together; 5 Outlook; Acknowledgements; References; 2 Kinetic and Thermodynamic Considerations in On-Surface Synthesis; Abstract; 1 Introduction; 2 Dehydrogenation Reactions; 3 Entropy of Desorbed Hydrogen Molecules; 4 Electrocyclic Ring-Closure Reaction; 5 C-H Activation and Coupling of Porphyrins; 6 Reaction Intermediates Stabilized by Surface Dissipation and Translational Entropy.

Text of Note

2.2 On-Surface Dehydrogenative Homocoupling2.3 Sequential C-X Groups Activation; 3 Summary and Outlook; References; 5 On-Surface Ullmann Reaction for the Synthesis of Polymers and Macrocycles; Abstract; 1 Introduction; 2 Synthesis of Polymers via Surface Ullmann Reaction; 2.1 The Emergence of the On-Surface Ullmann Reaction; 2.2 Identification of Organometallic Intermediates on Surfaces; 2.3 Stabilization of Organometallic Chains; 2.4 Dynamics of the Formation of Organometallic Chains; 2.5 Formation of Covalent Polymers; 3 Synthesis of Macrocycles via Surface Ullmann Reaction.

Text of Note

3.1 Cyclisation via Ring-Closure on a Surface3.2 Formation of Organometallic Macrocycles; 3.3 Formation of Covalent Macrocycles; 4 Summary; References; 6 Bottom-Up Fabrication of Atomically Precise Graphene Nanoribbons; Abstract; 1 Introduction; 2 Synthesis; 3 Characterization Tools and Associated Insight; 3.1 Electronic Properties Determination; 3.2 Chemical Structure; 3.3 Detection of Vibrational Modes; 4 Tuning the Electronic Properties; 4.1 Tuning Through Edge Orientation; 4.2 Tuning Through Width Control; 4.3 Tuning Through Doping; 4.4 Tuning Through Strain.

Text of Note

4.5 Tuning Through Heterostructure Formation5 Applications; Acknowledgements; References; 7 Aryl-Aryl Covalent Coupling on Rutile TiO2 Surfaces; Abstract; 1 Introduction; 2 TiO2 Properties; 2.1 General; 2.2 Comparison Between Rutile Faces; 2.3 Crystal Reduction and Surface Defects; 3 Aryl Halide Coupling on the Rutile (011) Surface; 3.1 First Successful C-C Coupling on a Rutile Surface; 3.2 Insight into Aryl Halide Coupling on the Rutile (011) Surface (Adapted from Ref. [18] with Permission from the Royal Chemical Society); 4 Aryl Halide Coupling on the Rutile (110) Surface.

Text of Note

7 Summary and OutlookReferences; 3 Reactivity on and of Graphene Layers: Scanning Probe Microscopy Reveals; Abstract; 1 Introduction; 2 Chemical Reactivity; 2.1 Synthesis of Imines; 2.2 Other Reactions; 3 Photochemical Reactivity; 4 Electrochemical Reactivity; 5 Tip-Induced Reactivity; 6 Graphene Manipulation and Grafting; 7 Summary and Conclusions; Acknowledgements; References; 4 Dehydrogenative and Dehalogenative Homocoupling Reactions of C-X Groups on Metal Surfaces; Abstract; 1 Introduction; 2 Results and Discussions; 2.1 On-Surface Dehalogenative Homocoupling.

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Text of Note

On-surface synthesis is appearing as an extremely promising strategy to create organic nanoarchitectures with atomic precision. Molecular building blocks holding adequate functional groups are dosed onto surfaces that support or even drive their covalent linkage. The surface confinement and the frequent lack of solvents (most commonly being performed under vacuum conditions) create a completely new scenario fully complementary to conventional chemistry. In a pedagogical way and based on the most recent developments, this volume presents our current understanding in the field, addressing fundamental reaction mechanisms, synthetic strategies to influence the reactions according to our needs, as well as the ultimate growth and characterization of functional materials. Verging on chemistry, physics and materials science, the book is aimed at students and researchers interested in nanochemistry, surface science, supramolecular materials and molecular devices. Chapters "Mechanistic insights into surface-supported chemical reactions", "Reactivity on and of Graphene Layers: Scanning Probe Microscopy Reviels" and "Bottom-up fabrication of atomically precise graphene nanoribbons" of this book are available open access under a CC BY 4.0 license at link.springer.com.

Source for Acquisition/Subscription Address

Springer Nature

Stock Number

com.springer.onix.9783319758107

Title

On-surface synthesis II.

International Standard Book Number

9783319758091

Parallel Title

On-surface synthesis 2

Nanochemistry, Congresses.

Nanostructured materials, Congresses.

Self-assembly (Chemistry), Congresses.

Surface chemistry, Congresses.

Materials science.

Nanochemistry.

Nanostructured materials.

Nanotechnology.

Organic chemistry.

Polymer chemistry.

Quantum & theoretical chemistry.

SCIENCE-- Chemistry-- Physical & Theoretical.

Self-assembly (Chemistry)

Surface chemistry.

SCI-- 013050

TBN

Number

Edition

Class number

Oteyza, Dimas G. de

Rogero, Celia

International Workshop On-Surface Synthesis(2016 :, San Sebastián, Spain)

Date of Transaction

20200823110332.0

Cataloguing Rules (Descriptive Conventions))

pn

Electronic name

[Book]

Y