@article{33681,
  author       = {{da Silva, Marcos A.R. and Silva, Ingrid F. and Xue, Qi and Lo, Benedict T.W. and Tarakina, Nadezda V. and Nunes, Barbara N. and Adler, Peter and Sahoo, Sudhir K. and Bahnemann, Detlef W. and López-Salas, Nieves and Savateev, Aleksandr and Ribeiro, Caue and Kühne, Thomas and Antonietti, Markus and Teixeira, Ivo F.}},
  issn         = {{0926-3373}},
  journal      = {{Applied Catalysis B: Environmental}},
  keywords     = {{Process Chemistry and Technology, General Environmental Science, Catalysis}},
  publisher    = {{Elsevier BV}},
  title        = {{{Sustainable oxidation catalysis supported by light: Fe-poly (heptazine imide) as a heterogeneous single-atom photocatalyst}}},
  doi          = {{10.1016/j.apcatb.2021.120965}},
  volume       = {{304}},
  year         = {{2021}},
}

@article{33675,
  abstract     = {{<jats:p>The influence of different polymer side chains on the vapor phase infiltration with TMA is investigated and supported by DFT-calculations.</jats:p>}},
  author       = {{Mai, Lukas and Maniar, Dina and Zysk, Frederik and Schöbel, Judith and Kühne, Thomas and Loos, Katja and Devi, Anjana}},
  issn         = {{1477-9226}},
  journal      = {{Dalton Transactions}},
  keywords     = {{Inorganic Chemistry}},
  number       = {{4}},
  pages        = {{1384--1394}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Influence of different ester side groups in polymers on the vapor phase infiltration with trimethyl aluminum}}},
  doi          = {{10.1039/d1dt03753f}},
  volume       = {{51}},
  year         = {{2021}},
}

@article{47963,
  abstract     = {{Nonlinear and quantum optical devices based on periodically-poled thin film lithium niobate (PP-TFLN) have gained considerable interest lately, due to their significantly improved performance as compared to their bulk counterparts. Nevertheless, performance parameters such as conversion efficiency, minimum pump power, and spectral bandwidth strongly depend on the quality of the domain structure in these PP-TFLN samples, e.g., their homogeneity and duty cycle, as well as on the overlap and penetration depth of domains with the waveguide mode. Hence, in order to propose improved fabrication protocols, a profound quality control of domain structures is needed that allows quantifying and thoroughly analyzing these parameters. In this paper, we propose to combine a set of nanometer-to-micrometer-scale imaging techniques, i.e., piezoresponse force microscopy (PFM), second-harmonic generation (SHG), and Raman spectroscopy (RS), to access the relevant and crucial sample properties through cross-correlating these methods. Based on our findings, we designate SHG to be the best-suited standard imaging technique for this purpose, in particular when investigating the domain poling process in x-cut TFLNs. While PFM is excellently recommended for near-surface high-resolution imaging, RS provides thorough insights into stress and/or defect distributions, as associated with these domain structures. In this context, our work here indicates unexpectedly large signs for internal fields occurring in x-cut PP-TFLNs that are substantially larger as compared to previous observations in bulk LN.}},
  author       = {{Reitzig, Sven and Rüsing, Michael and Zhao, Jie and Kirbus, Benjamin and Mookherjea, Shayan and Eng, Lukas M.}},
  issn         = {{2073-4352}},
  journal      = {{Crystals}},
  keywords     = {{Inorganic Chemistry, Condensed Matter Physics, General Materials Science, General Chemical Engineering}},
  number       = {{3}},
  publisher    = {{MDPI AG}},
  title        = {{{“Seeing Is Believing”—In-Depth Analysis by Co-Imaging of Periodically-Poled X-Cut Lithium Niobate Thin Films}}},
  doi          = {{10.3390/cryst11030288}},
  volume       = {{11}},
  year         = {{2021}},
}

@article{47964,
  abstract     = {{In the last two decades, variably doped strontium barium niobate (SBN) has attracted a lot of scientific interest mainly due to its specific non-linear optical response. Comparably, the parental compound, i.e., undoped SBN, appears to be less studied so far. Here, two different cuts of single-crystalline nominally pure strontium barium niobate in the composition Sr0.61Ba0.39Nb2O6 (SBN61) are comprehensively studied and analyzed with regard to their photoconductive responses. We present conductance measurements under systematically varied illumination conditions along either the polar z-axis or perpendicular to it (x-cut). Apart from a pronounced photoconductance (PC) already under daylight and a large effect upon super-bandgap illumination in general, we observe (i) distinct spectral features when sweeping the excitation wavelength over the sub-bandgap region as then discussed in the context of deep and shallow trap states, (ii) extremely slow long-term relaxation for both light-on and light-off transients in the range of hours and days, (iii) a critical dependence of the photoresponse on the pre-illumination history of the sample, and (iv) a current–voltage hysteresis depending on both the illumination and the electrical-measurement conditions in a complex manner.}},
  author       = {{Beyreuther, Elke and Ratzenberger, Julius and Roeper, Matthias and Kirbus, Benjamin and Rüsing, Michael and Ivleva, Liudmila I. and Eng, Lukas M.}},
  issn         = {{2073-4352}},
  journal      = {{Crystals}},
  keywords     = {{Inorganic Chemistry, Condensed Matter Physics, General Materials Science, General Chemical Engineering}},
  number       = {{7}},
  publisher    = {{MDPI AG}},
  title        = {{{Photoconduction of Polar and Nonpolar Cuts of Undoped Sr0.61Ba0.39Nb2O6 Single Crystals}}},
  doi          = {{10.3390/cryst11070780}},
  volume       = {{11}},
  year         = {{2021}},
}

@article{47965,
  abstract     = {{Exceptionally electron-rich, nearly trigonal-planar tricyanidometalate anions [Fe(CN)3]7− and [Ru(CN)3]7− were stabilized in LiSr3[Fe(CN)3] and AE3.5[M(CN)3] (AE=Sr, Ba; M=Fe, Ru). They are the first examples of group 8 elements with the oxidation state of −IV. Microcrystalline powders were obtained by a solid-state route, single crystals from alkali metal flux. While LiSr3[Fe(CN)3] crystallizes in P63/m, the polar space group P63 with three-fold cell volume for AE3.5[M(CN)3] is confirmed by second harmonic generation. X-ray diffraction, IR and Raman spectroscopy reveal longer C−N distances (124–128 pm) and much lower stretching frequencies (1484–1634 cm−1) than in classical cyanidometalates. Weak C−N bonds in combination with strong M−C π-bonding is a scheme also known for carbonylmetalates. Instead of the formal notation [Fe−IV(CN−)3]7−, quantum chemical calculations reveal non-innocent intermediate-valent CN1.67− ligands and a closed-shell d10 configuration for Fe, that is, Fe2−.}},
  author       = {{Jach, Franziska and Wagner, Frank R. and Amber, Zeeshan H. and Rüsing, Michael and Hunger, Jens and Prots, Yurii and Kaiser, Martin and Bobnar, Matej and Jesche, Anton and Eng, Lukas M. and Ruck, Michael and Höhn, Peter}},
  issn         = {{1433-7851}},
  journal      = {{Angewandte Chemie International Edition}},
  keywords     = {{General Chemistry, Catalysis}},
  number       = {{29}},
  pages        = {{15879--15885}},
  publisher    = {{Wiley}},
  title        = {{{Tricyanidoferrates(−IV) and Ruthenates(−IV) with Non‐Innocent Cyanido Ligands}}},
  doi          = {{10.1002/anie.202103268}},
  volume       = {{60}},
  year         = {{2021}},
}

@article{47977,
  abstract     = {{Orange-colored crystals of the oxoferrate tellurate K12+6xFe6Te4−xO27 [x=0.222(4)] were synthesized in a potassium hydroxide hydroflux with a molar water–base ratio n(H2O)/n(KOH) of 1.5 starting from Fe(NO3)3 ⋅ 9H2O, TeO2 and H2O2 at about 200 °C. By using (NH4)2TeO4 instead of TeO2, a fine powder consisting of microcrystalline spheres of K12+6xFe6Te4−xO27 was obtained. K12+6xFe6Te4−xO27 crystallizes in the acentric cubic space group Iurn:x-wiley:09476539:media:chem202102464:chem202102464-math-0001 3d. [FeIIIO5] pyramids share their apical atoms in [Fe2O9] groups and two of their edges with [TeVIO6] octahedra to form an open framework that consists of two loosely connected, but not interpenetrating, chiral networks. The flexibility of the hinged oxometalate network manifests in a piezoelectric response similar to that of LiNbO3.The potassium cations are mobile in channels that run along the <111> directions and cross in cavities acting as nodes. The ion conductivity of cold-pressed pellets of ball-milled K12+6xFe6Te4−xO27 is 2.3×10^(−4) S ⋅ cm^(−1) at room temperature. Magnetization measurements and neutron diffraction indicate antiferromagnetic coupling in the [Fe2O9] groups.}},
  author       = {{Albrecht, Ralf and Hoelzel, Markus and Beccard, Henrik and Rüsing, Michael and Eng, Lukas and Doert, Thomas and Ruck, Michael}},
  issn         = {{0947-6539}},
  journal      = {{Chemistry – A European Journal}},
  keywords     = {{General Chemistry, Catalysis, Organic Chemistry}},
  number       = {{57}},
  pages        = {{14299--14306}},
  publisher    = {{Wiley}},
  title        = {{{Potassium Ion Conductivity in the Cubic Labyrinth of a Piezoelectric, Antiferromagnetic Oxoferrate(III) Tellurate(VI)}}},
  doi          = {{10.1002/chem.202102464}},
  volume       = {{27}},
  year         = {{2021}},
}

@article{47569,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>The trend of increasing product diversity and decreasing production amounts led to the requirement of higher flexibility of production processes of specialty chemicals. Conventional distillation columns, mostly equipped with structured packings, lack the flexibility to handle product changeovers and throughput. Thus, a newly designed distillation column for specialty chemicals is presented. A numerical model was implemented to analyze the potential of the wetted‐wall column. The simulation of the distillation of a binary methanol/water mixture demonstrated that the wetted‐wall column can generate the desired concentration and temperature profiles. Furthermore, analyses of the pressure drop and separation efficiency with the test system chlorobenzene/ethylbenzene were conducted.</jats:p>}},
  author       = {{Reitze, Arnulf and Grünewald, Marcus and Riese, Julia}},
  issn         = {{0930-7516}},
  journal      = {{Chemical Engineering &amp; Technology}},
  keywords     = {{Industrial and Manufacturing Engineering, General Chemical Engineering, General Chemistry}},
  number       = {{7}},
  pages        = {{1327--1335}},
  publisher    = {{Wiley}},
  title        = {{{Concept of a Flexible Wetted‐Wall Column for the Distillation of Specialty Chemicals}}},
  doi          = {{10.1002/ceat.202000468}},
  volume       = {{44}},
  year         = {{2021}},
}

@article{47564,
  author       = {{Reitze, Arnulf and Grünewald, Marcus and Riese, Julia}},
  issn         = {{0888-5885}},
  journal      = {{Industrial &amp; Engineering Chemistry Research}},
  keywords     = {{Industrial and Manufacturing Engineering, General Chemical Engineering, General Chemistry}},
  number       = {{1}},
  pages        = {{740--746}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Characterization of Liquid-Phase Distribution in 3D Printed Structured Packings with an Enclosed Column Wall}}},
  doi          = {{10.1021/acs.iecr.1c03931}},
  volume       = {{61}},
  year         = {{2021}},
}

@article{47567,
  author       = {{Bruns, Bastian and Di Pretoro, Alessandro and Grünewald, Marcus and Riese, Julia}},
  issn         = {{0009-2509}},
  journal      = {{Chemical Engineering Science}},
  keywords     = {{Applied Mathematics, Industrial and Manufacturing Engineering, General Chemical Engineering, General Chemistry}},
  publisher    = {{Elsevier BV}},
  title        = {{{Flexibility analysis for demand-side management in large-scale chemical processes: An ethylene oxide production case study}}},
  doi          = {{10.1016/j.ces.2021.116779}},
  volume       = {{243}},
  year         = {{2021}},
}

@article{47565,
  author       = {{Bruns, Bastian and Di Pretoro, Alessandro and Grünewald, Marcus and Riese, Julia}},
  issn         = {{0888-5885}},
  journal      = {{Industrial &amp; Engineering Chemistry Research}},
  keywords     = {{Industrial and Manufacturing Engineering, General Chemical Engineering, General Chemistry}},
  number       = {{1}},
  pages        = {{605--620}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Indirect Demand Response Potential of Large-Scale Chemical Processes}}},
  doi          = {{10.1021/acs.iecr.1c03925}},
  volume       = {{61}},
  year         = {{2021}},
}

@article{47568,
  author       = {{Bruns, Bastian and Herrmann, Felix and Grünewald, Marcus and Riese, Julia}},
  issn         = {{0888-5885}},
  journal      = {{Industrial &amp; Engineering Chemistry Research}},
  keywords     = {{Industrial and Manufacturing Engineering, General Chemical Engineering, General Chemistry}},
  number       = {{20}},
  pages        = {{7678--7688}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Dynamic Design Optimization for Flexible Process Equipment}}},
  doi          = {{10.1021/acs.iecr.1c00306}},
  volume       = {{60}},
  year         = {{2021}},
}

@article{47570,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Shortened product life cycles and increased demand for specialized products lead to more challenges in efficiently satisfying customer needs. Customer demands are increasingly uncertain in terms of type, location, and volume. As a result, more flexible chemical production plants are required. Modular small‐scale plants can be installed in transportation containers and, therefore, offer the flexibility of easy relocation, enabling production close to the customer or supplier. In a mathematical optimization model, the economic benefit of small‐scale plants in the specialty chemicals market of polymer production is analyzed. Different scenarios created from the real data of a chemical company show that the use of small‐scale plants may lead to a significant reduction in total costs that is mainly due to the transportation costs of raw materials and products.</jats:p>}},
  author       = {{Bruns, Bastian and Becker, Tristan and Riese, Julia and Lier, Stefan and Werners, Brigitte}},
  issn         = {{0930-7516}},
  journal      = {{Chemical Engineering &amp; Technology}},
  keywords     = {{Industrial and Manufacturing Engineering, General Chemical Engineering, General Chemistry}},
  number       = {{6}},
  pages        = {{1148--1152}},
  publisher    = {{Wiley}},
  title        = {{{Efficient Production of Specialized Polymers with Highly Flexible Small‐Scale Plants}}},
  doi          = {{10.1002/ceat.202000591}},
  volume       = {{44}},
  year         = {{2021}},
}

@article{47571,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>Im Rahmen dieses Beitrags werden experimentelle Untersuchungen zur Tropfenabscheidung im Einleitbereich eines Stoffaustauschapparates für zweiphasige Strömungen vorgestellt. Dafür wurde in einem Versuchsstand im Pilotmaßstab der qualitative Tropfenmitriss für unterschiedliche Tropfenabscheider eines Stoffaustauschapparates vermessen. Die daraus resultierenden Ergebnisse werden in diesem Beitrag hinsichtlich ihrer Aussagekraft zur Vermeidung von Tropfenmitriss diskutiert und bewertet. Darüber hinaus wird ein kurzer Ausblick über simulative Arbeiten zur Bestimmung des Tropfenmitriss gegeben.</jats:p>}},
  author       = {{Fasel, Henrik and Darvishsefat, Novin and Riese, Julia and Grünewald, Marcus}},
  issn         = {{0009-286X}},
  journal      = {{Chemie Ingenieur Technik}},
  keywords     = {{Industrial and Manufacturing Engineering, General Chemical Engineering, General Chemistry}},
  number       = {{7}},
  pages        = {{1100--1106}},
  publisher    = {{Wiley}},
  title        = {{{Experimentelle Untersuchungen zum Tropfenmitriss im Feedeinleitbereich von Destillationskolonnen}}},
  doi          = {{10.1002/cite.202000242}},
  volume       = {{93}},
  year         = {{2021}},
}

@article{53086,
  author       = {{Zhang, Hao and Kaczmarek, Dennis and Rudolph, Charlotte and Schmitt, Steffen and Gaiser, Nina and Oßwald, Patrick and Bierkandt, Thomas and Kasper, Tina and Atakan, Burak and Kohse-Höinghaus, Katharina}},
  issn         = {{0010-2180}},
  journal      = {{Combustion and Flame}},
  keywords     = {{General Physics and Astronomy, Energy Engineering and Power Technology, Fuel Technology, General Chemical Engineering, General Chemistry}},
  publisher    = {{Elsevier BV}},
  title        = {{{Dimethyl ether (DME) and dimethoxymethane (DMM) as reaction enhancers for methane: Combining flame experiments with model-assisted exploration of a polygeneration process}}},
  doi          = {{10.1016/j.combustflame.2021.111863}},
  volume       = {{237}},
  year         = {{2021}},
}

@article{53085,
  author       = {{Gaiser, Nina and Bierkandt, Thomas and Oßwald, Patrick and Zinsmeister, Julia and Kathrotia, Trupti and Shaqiri, Shkelqim and Hemberger, Patrick and Kasper, Tina and Aigner, Manfred and Köhler, Markus}},
  issn         = {{0016-2361}},
  journal      = {{Fuel}},
  keywords     = {{Organic Chemistry, Energy Engineering and Power Technology, Fuel Technology, General Chemical Engineering}},
  publisher    = {{Elsevier BV}},
  title        = {{{Oxidation of oxymethylene ether (OME0−5): An experimental systematic study by mass spectrometry and photoelectron photoion coincidence spectroscopy}}},
  doi          = {{10.1016/j.fuel.2021.122650}},
  volume       = {{313}},
  year         = {{2021}},
}

@article{41001,
  abstract     = {{For entropic reasons, the synthesis of macrocycles via olefin ring-closing metathesis (RCM) is impeded by competing acyclic diene metathesis (ADMET) oligomerization. With cationic molybdenum imido alkylidene N-heterocyclic carbene (NHC) complexes confined in tailored ordered mesoporous silica, RCM can be run with macrocyclization selectivities up to 98% and high substrate concentrations up to 0.1 M. Molecular dynamics simulations show that the high conversions are a direct result of the proximity between the surface-bound catalyst, proven by extended X-ray absorption spectroscopy, and the surface-located substrates. Back-diffusion of the macrocycles decreases with decreasing pore diameter of the silica and is responsible for the high macrocyclization efficiency. Also, Z-selectivity increases with decreasing pore diameter and increasing Tolman electronic parameter of the NHC. Running reactions at different concentrations allows for identifying the optimum substrate concentration for each material and substrate combination.}},
  author       = {{Ziegler, Felix and Kraus, Hamzeh and Benedikter, Mathis J. and Wang, Dongren and Bruckner, Johanna R. and Nowakowski, Michał and Weißer, Kilian and Solodenko, Helena and Schmitz, Guido and Bauer, Matthias and Hansen, Niels and Buchmeiser, Michael R.}},
  issn         = {{2155-5435}},
  journal      = {{ACS Catalysis}},
  keywords     = {{Catalysis, General Chemistry}},
  number       = {{18}},
  pages        = {{11570--11578}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Confinement Effects for Efficient Macrocyclization Reactions with Supported Cationic Molybdenum Imido Alkylidene <i>N</i>-Heterocyclic Carbene Complexes}}},
  doi          = {{10.1021/acscatal.1c03057}},
  volume       = {{11}},
  year         = {{2021}},
}

@article{40999,
  abstract     = {{Rh(I) NHC and Rh(III) Cp* NHC complexes (Cp*=pentamethylcyclopentadienyl, NHC=N-heterocyclic carbene=pyrid-2-ylimidazol-2-ylidene (Py−Im), thiophen-2-ylimidazol-2-ylidene) are presented. Selected catalysts were selectively immobilized inside the mesopores of SBA-15 with average pore diameters of 5.0 and 6.2 nm. Together with their homogenous progenitors, the immobilized catalysts were used in the hydrosilylation of terminal alkynes. For aromatic alkynes, both the neutral and cationic Rh(I) complexes showed excellent reactivity with exclusive formation of the β(E)-isomer. For aliphatic alkynes, however, selectivity of the Rh(I) complexes was low. By contrast, the neutral and cationic Rh(III) Cp* NHC complexes proved to be highly regio- and stereoselective catalysts, allowing for the formation of the thermodynamically less stable β-(Z)-vinylsilane isomers at room temperature. Notably, the SBA-15 immobilized Rh(I) catalysts, in which the pore walls provide an additional confinement, showed excellent β-(Z)-selectivity in the hydrosilylation of aliphatic alkynes, too. Also, in the case of 4-aminophenylacetylene, selective formation of the β(Z)-isomer was observed with a neutral SBA-15 supported Rh(III) Cp* NHC complex but not with its homogenous counterpart. These are the first examples of high β(Z)-selectivity in the hydrosilylation of alkynes by confinement generated upon immobilization inside mesoporous silica.}},
  author       = {{Panyam, Pradeep K. R. and Atwi, Boshra and Ziegler, Felix and Frey, Wolfgang and Nowakowski, Michał and Bauer, Matthias and Buchmeiser, Michael R.}},
  issn         = {{0947-6539}},
  journal      = {{Chemistry – A European Journal}},
  keywords     = {{General Chemistry, Catalysis, Organic Chemistry}},
  number       = {{68}},
  pages        = {{17220--17229}},
  publisher    = {{Wiley}},
  title        = {{{Rh(I)/(III)‐N‐Heterocyclic Carbene Complexes: Effect of Steric Confinement Upon Immobilization on Regio‐ and Stereoselectivity in the Hydrosilylation of Alkynes}}},
  doi          = {{10.1002/chem.202103099}},
  volume       = {{27}},
  year         = {{2021}},
}

@article{41009,
  abstract     = {{Platinum hydride species catalyze a number of interesting organic reactions. However, their reactions typically involve the use of high loadings of noble metal and are difficult to recycle, making them somewhat unsustainable. We have synthesized surface-immobilized Pt–H species via oxidative addition of surface OH groups to Pt(PtBu3)2 (1), a rarely used immobilization technique in surface organometallic chemistry. The hydride species thus made were characterized by infrared, magic-angle spinning nuclear magnetic resonance, and X-ray absorption spectroscopies and catalyzed both olefin isomerization and cycloisomerization of a 1,6 enyne (5) with a high selectivity and low Pt loading.}},
  author       = {{Maier, Sarah and Cronin, Steve P. and Vu Dinh, Manh-Anh and Li, Zheng and Dyballa, Michael and Nowakowski, Michał and Bauer, Matthias and Estes, Deven P.}},
  issn         = {{0276-7333}},
  journal      = {{Organometallics}},
  keywords     = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry}},
  number       = {{11}},
  pages        = {{1751--1757}},
  publisher    = {{American Chemical Society (ACS)}},
  title        = {{{Immobilized Platinum Hydride Species as Catalysts for Olefin Isomerizations and Enyne Cycloisomerizations}}},
  doi          = {{10.1021/acs.organomet.1c00216}},
  volume       = {{40}},
  year         = {{2021}},
}

@article{30216,
  author       = {{Huber-Gedert, Marina and Nowakowski, Michał and Kertmen, Ahmet and Burkhardt, Lukas and Lindner, Natalia and Schoch, Roland and Herbst‐Irmer, Regine and Neuba, Adam and Schmitz, Lennart and Choi, Tae‐Kyu and Kubicki, Jacek and Gawelda, Wojciech and Bauer, Matthias}},
  issn         = {{0947-6539}},
  journal      = {{Chemistry – A European Journal}},
  keywords     = {{Photocatalytic Hydrogen Production, Catalysis, Inorganic Chemistry}},
  number       = {{38}},
  pages        = {{9905--9918}},
  publisher    = {{Wiley}},
  title        = {{{Fundamental Characterization, Photophysics and Photocatalysis of a Base Metal Iron(II)‐Cobalt(III) Dyad}}},
  doi          = {{10.1002/chem.202100766}},
  volume       = {{27}},
  year         = {{2021}},
}

@article{35686,
  abstract     = {{<jats:title>Abstract</jats:title><jats:p>The development of the frustrated Lewis pair catalyzed hydrogenation of tertiary and secondary amides is reviewed. Detailed insight into our strategies in order to overcome challenges during the reaction development process is provided. Furthermore, the developed chemistry is extended to the hydrogenation of polyamides and of trifluoroacetamides for the convenient introduction of trifluoroethyl groups into organic molecules.</jats:p>}},
  author       = {{Paradies, Jan and Köring, Laura and Sitte, Nikolai A.}},
  issn         = {{0039-7881}},
  journal      = {{Synthesis}},
  keywords     = {{Organic Chemistry, Catalysis}},
  number       = {{05}},
  pages        = {{1287--1300}},
  publisher    = {{Georg Thieme Verlag KG}},
  title        = {{{Towards the Development of Frustrated Lewis Pair (FLP) Catalyzed Hydrogenations of Tertiary and Secondary Carboxylic Amides}}},
  doi          = {{10.1055/a-1681-3972}},
  volume       = {{54}},
  year         = {{2021}},
}