• No results found

University of Groningen Control of translational and rotational movement at nanoscale Stacko, Peter

N/A
N/A
Protected

Academic year: 2021

Share "University of Groningen Control of translational and rotational movement at nanoscale Stacko, Peter"

Copied!
3
0
0

Bezig met laden.... (Bekijk nu de volledige tekst)

Hele tekst

(1)

University of Groningen

Control of translational and rotational movement at nanoscale

Stacko, Peter

IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from

it. Please check the document version below.

Document Version

Publisher's PDF, also known as Version of record

Publication date:

2017

Link to publication in University of Groningen/UMCG research database

Citation for published version (APA):

Stacko, P. (2017). Control of translational and rotational movement at nanoscale. University of Groningen.

Copyright

Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons).

Take-down policy

If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim.

Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum.

(2)

Stellingen

behorende bij het proefschrift

“Control of Translational and Rotational Movement at Nanoscale” door

Peter Štacko

1. Negative results and failed attempts should be reported in literature more often since it could often greatly speed up or improve the follow-up research. 2. The fact that previous attempts in the literature to synthesize a compound

failed does not mean you cannot synthesize it following the exact same method (Chapter 3).

3. In academic settings, researchers are overly reliant on column chromatography as a purification method, while often more suitable techniques are available (especially for large quantities).

4. The melting point does not provide any useful information regarding the identity of the compound, especially when taking into account the influence of omnipresent impurities such as water and the existence of polymorphs. 5. It should not be possible to publish a photochemical paper without a single

UV-vis spectrum, especially when a novel photochemical transformation is reported without any prior references to such process.

Org. Lett. 2017, 19, 4822-4825

6. The names of the referees who reviewed a paper should be reported along with the list of the authors.

7. If the experimental details on the synthesis of the only molecule studied are not reported, but referenced to another paper, in which no such molecule is reported, one might wonder what molecule the authors were actually investigating.

(3)

8. Drawing conclusions based on the comparison of two numbers within one order of magnitude (for instance half-lives of the metastable states of molecular motors) is meaningless unless you provide some sort of statistical information (i.e. standard error) and understand how these numbers are mathematically produced.

Referenties

GERELATEERDE DOCUMENTEN

Chapter V: Geared movement of a biaryl system controlled by a molecular motor Introduction

The previous sections address both biological motors as well as artificial molecular motors starting with rotaxane and catenane based systems, followed by chemically and

Molecular dragsters bearing two appending molecular motor units as the propelling wheels have been synthesized. The two dragsters feature different sizes of the

In order to verify the hypothesis that installation of the fluorine atom at the stereogenic center leads to a large increase of the barrier for thermal helix

Design and synthesis of p-xylene based third generation motors The design of the achiral molecular motor system (Figure 2) is based on second generation rotary motors 37,39

biaryl bond during the photochemical E-Z isomerization (i.e. a single face of the aryl keeps facing the lower half), however, it is not excluded that the helicity of the biaryl

The solvents were evaporated at reduced pressure and the residue purified by flash column chromatography (pentane : ethyl acetate – 3 : 1) to give the title product

Having concluded that installing substituents on the parent compound 7.1 leads to substantially slower fluorescence decay and longer fluorescence lifetimes, but further increasing