G. Alexander Groß

Dr. G. Alexander Groß

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Research Focus & Metrics

Academic Career Length

21Years (2006-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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31 January 2011 in Chemistry – A European Journal
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Journal Article
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LALahbib Abahmane
Lahbib Abahmane
JKJ. Michael Köhler
J. Michael Köhler
GGG. Alexander Groß
G. Alexander Groß

28 February 2007 in Chemical Engineering & Technology
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Journal Article
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GGG. Alexander Groß
G. Alexander Groß
CHC. Hamann
C. Hamann
PGP. M. Günther
P. M. Günther
JKJ. M. Köhler
J. M. Köhler

29 October 2009 in Chemical Engineering & Technology
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Journal Article
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LAL. Abahmane
L. Abahmane
AKA. Knauer
A. Knauer
URU. Ritter
U. Ritter
JKJ. M. Köhler
J. M. Köhler
GGG. Alexander Groß
G. Alexander Groß

8 June 2020 in Micromachines
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Journal Article
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Jialan CaoJialan Cao
Jialan Cao
FRFelix Richter
Felix Richter
MKMichael Kastl
Michael Kastl
JEJonny Erdmann
Jonny Erdmann
CBChristian Burgold
Christian Burgold
GGG. Alexander Groß
G. Alexander Groß
Droplet-based microfluidics is a versatile tool to reveal the dose–response relationship of different effectors on the microbial proliferation. Traditional readout parameter is the temporal development of the cell density for different effector concentrations. To determine nonlinear or unconventional dose–response relationships, data with high temporal resolution and dense concentration graduation are essential. If microorganisms with slow microbial growth kinetics are investigated, a sterile and evaporation-free long-term incubation technique is required. Here, we present a modular droplet-based screening system which was developed to solve these issues. Beside relevant technical aspects of the developed modules, the procedural workflow, and exemplary dose–response data for 1D and 2D dose–response screenings are presented.

25 August 2011 in Beilstein Journal of Organic Chemistry
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Journal Article
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SSSukhdeep Singh
Sukhdeep Singh
JKJ. Michael Köhler
J. Michael Köhler
ASAndreas Schober
Andreas Schober
GGG. Alexander Groß
G. Alexander Groß
The Eschenmoser coupling is a useful carbon–carbon bond forming reaction which has been used in various different synthesis strategies. The reaction proceeds smoothly if S-alkylated ternary thioamides or thiolactames are used. In the case of S-alkylated secondary thioamides or thiolactames, the Eschenmoser coupling needs prolonged reaction times and elevated temperatures to deliver valuable yields. We have used a flow chemistry system to promote the Eschenmoser coupling under enhanced reaction conditions in order to convert the demanding precursors such as S-alkylated secondary thioamides and thiolactames in an efficient way. Under pressurized reaction conditions at about 220 °C, the desired Eschenmoser coupling products were obtained within 70 s residence time. The reaction kinetics was investigated and 15 examples of different building block combinations are given.

23 April 2023 in Polymers
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AHAntonella Hadzich
Antonella Hadzich
SFSantiago Flores
Santiago Flores
AMAshley Masucci
Ashley Masucci
EGEnrique D Gomez
Enrique D Gomez
GGG. Alexander Groß
G. Alexander Groß
Alkyd resins are oil-based polymers that have been widely used for generations in the surface coating industry and beyond. Characterization of these resins is of high importance to understand the influence of its components on its behavior, compatibility with other resins, and final quality to ensure high durability. Here, NMR spectroscopy and GPC were used for characterizing differences in the chemical structure, molecular distribution, and dispersity between oil-based and fatty acid-based alkyd polymers made from sacha inchi and linseed oils. Sancha inchi (Plukentia volubilis L.) is a fruit-bearing plant native to South America and the Caribbean, and has a rich unsaturated fatty acid content. The effect of vegetable oil and polyol selection on the synthesis of alkyd resins for coating applications was analyzed. The influence of two different synthesis methods, monoglyceride and fatty acid processes, was also compared. Important structural differences were observed using NMR: one-dimensional spectra revealed the degree of unsaturated fatty acid chains along the polyester backbone, whereas, 2D NMR experiments facilitated chemical shift assignments of all signals. GPC analysis suggested that alkyd resins with homogeneous and high molecular weights can be obtained with the fatty acid process, and that resins containing pentaerythritol may have uniform chain lengths.