0000000001300595
AUTHOR
Arne Lützen
showing 76 related works from this author
Anion binding to resorcinarene-based cavitands: the importance of C-H...anion interactions.
2008
Frontispiece: An Octanuclear Metallosupramolecular Cage Designed To Exhibit Spin-Crossover Behavior
2017
Electron-Deficient Pyridylimines: Versatile Building Blocks for Functional Metallosupramolecular Chemistry
2017
Metallosupramolecular systems heavily rely on the correct choice of ligands to obtain materials with desired properties. Engaging this problem, we present three ligand systems and six of their mono- and dinuclear complexes, based on the subcomponent self-assembly approach using electron-deficient pyridylcarbaldehyde building blocks. The properties are examined in solution by NMR and UV-vis spectroscopy and CV measurements as well as in solid state by single crystal X-ray diffraction analysis. Ultimately, the choice of ligands allows for fine-tuning of the electronic properties of the metal centers, complex-to-complex transformations, as well as establishing distinct anion-π-interaction moti…
Self-assembly of metallosupramolecular rhombi from chiral concave 9,9'-spirobifluorene-derived bis(pyridine) ligands.
2014
Two new 9,9’-spirobifluorene-based bis(4-pyridines) were synthesised in enantiopure and one also in racemic form. These ligands act as concave templates and form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. The self-assembly process of the racemic ligand preferably occurs in a narcissistic self-recognising manner. Hence, a mixture of all three possible stereoisomers [(dppp)2M2{(R)-L}2](OTf)4, [(dppp)2M2{(S)-L}2](OTf)4, and [(dppp)2M2{(R)-L}{(S)-L}](OTf)4 was obtained in an approximate 1.5:1.5:1 ratio which corresponds to an amplification of the homochiral assemblies by a factor of approximately three as evidenced by NMR spectroscopy and m…
Ein achtkerniger metallosupramolekularer Würfel mit Spin-Crossover-Eigenschaften
2017
Self-Sorting Effects in the Self-Assembly of Metallosupramolecular Rhombi from Chiral BINOL-Derived Bis(pyridine) Ligands
2013
Four BINOL-based bis(4-pyridyl) ligands were synthesised in enantiopure and racemic form. These ligands form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. In principle, racemic ligands can self-assemble into three stereoisomeric rhombi. The degree of self-sorting in the self-assembly process crucially depends on the substitution pattern and the resulting bend angle of the V-shaped ligands as well as the degree of steric crowding within the assembly when racemic ligands are used. Thus, these processes either lead to homochiral assemblies in a narcissistic self-recognition manner, to heterochiral assemblies in a social self-discriminating ma…
A New Structural Motif for an Enantiomerically Pure Metallosupramolecular Pd4L8Aggregate by Anion Templating
2014
An enantiomerically pure BINOL-based bis(3-pyridyl) ligand 1 assembles into a homochiral [Pd4(1)8] complex upon coordination to tetravalent PdII ions. The formation of this aggregate is templated by two tetrafluoroborate counterions that are encapsulated in two peripheral cavities. The resulting structure is a new structural motif for this kind of metallosupramolecular assemblies that arranges the palladium ions in a distorted tetrahedral fashion and forces ligand 1 to adopt two different conformations. Both phenomena are unique and cause an overall three-dimensional structure that has another confined, chiral, and hydrophilic central cavity.
Enantiomerenreine [M6L12]- oder [M12L24]-Polyeder aus flexiblen Bis(pyridin)-Liganden
2014
Enantiomerically pure [M(6)L(12)] or [M(12)L(24)] polyhedra from flexible bis(pyridine) ligands.
2013
Coordination-driven self-assembly is one of the most powerful strategies to prepare nanometer-sized discrete (supra)molecular assemblies. Herein, we report on the use of two constitutionally isomeric BINOL-based bis(pyridine) ligands for this purpose. Upon coordination to Pd(II) ions these self-assemble into enantiomerically pure endo- and exo-functionalized hexa- and dodecanuclear metallosupramolecular spheres with a chiral skeleton depending on the substitution pattern of the BINOL core. These aggregates were characterized by NMR, MS, DLS, TEM, and EELS as well as ECD. Furthermore, experimental ECD data could be compared to those obtained from theoretical simulations using a simplified Ta…
New Carbaalanes − (AlMe)8(CCH2Me)5(C≡C−Me) and the THF Adduct (AlMe)8(CCH2Me)5H·2THF
2001
The hydroalumination of Me2Al−C≡C−Me with a large excess of Me2AlH afforded the arachno-carbaalane (AlMe)8(CCH2Me)5H (4) by the release of AlMe3. 4 is almost insoluble in noncoordinating solvents and could not be purified by recrystallization. On an attempt to recrystallize 4 from a THF solution, the adduct (AlMe)8(CCH2Me)5H·2THF (5) was isolated as the first stable ether adduct of a carbaalane. Crystal structure determination revealed a cube of eight aluminium atoms, five faces of which are bridged by C−CH2Me groups. The sixth face is µ2-bridged by a hydrogen atom, and two opposite aluminium atoms of this face are coordinated by one THF ligand each. When the excess of dimethylaluminium hyd…
Simultane endo - und exo -Komplexbildung von Pyridin[4]aren-Dimeren mit neutralen und anionischen Gästen
2017
Chiral Self‐Sorting of trans ‐Chelating Chiral Ligands upon Formation of Pd II Complexes (Eur. J. Inorg. Chem. 15/2014)
2014
Equipping metallo-supramolecular macrocycles with functional groups: Assemblies of pyridine-substituted urea ligands
2012
A series of di-(m-pyridyl)-urea ligands were prepared and characterized with respect to their conformations by NOESY experiments and crystallography. Methyl substitution in different positions of the pyridine rings provides control over the position of the pyridine N atoms relative to the urea carbonyl group. The ligands were used to self-assemble metallo-supramolecular M(2)L(2) and M(3)L(3) macrocycles which are generated in a finely balanced equilibrium in DMSO and DMF according to DOSY NMR experiments and ESI FTICR mass spectrometry. Again, crystallography was used to characterize the assemblies. Methyl substitution in positions next to the pyridine nitrogen prevents coordination, while …
Enantiomerically pure trinuclear helicates via diastereoselective self-assembly and characterization of their redox chemistry.
2014
A tris(bipyridine) ligand 1 with two BINOL (BINOL = 2, 2′-dihydroxy-1, 1′-binaphthyl) groups has been prepared in two enantiomerically pure forms. This ligand undergoes completely diastereoselective self-assembly into D2-symmeteric double-stranded trinuclear helicates upon coordination to copper(I) and silver(I) ions and to D3-symmetric triple-stranded trinuclear helicates upon coordination to copper(II), zinc(II), and iron(II) ions as demonstrated by mass spectrometry, NMR and CD spectroscopy in combination with quantum chemical calculations and X-ray diffraction analysis. According to the calculations, the single diastereomers that are formed during the self-assembly process are strongly …
Anionen bindende Resorcinaren-Cavitanden: die Bedeutung von CH⋅⋅⋅Anion-Wechselwirkungen
2008
Unexpected self-assembly of a homochiral metallosupramolecular M4L4 catenane
2014
Two enantiomerically pure 9,9'-spirobifluorene-based bis(pyridine) ligands 1 and 2 were prepared to study their self-assembly behavior upon coordination to cis-protected palladium(II) ions. Whereas the sterically more demanding ligand, 2, gave rise to the expected dinuclear metallosupramolecular M2L2 rhombi, the sterically less demanding ligand, 1, acts as a template to give rise to a homochiral metallosupramolecular M4L4 catenane.
Thermodynamically driven self-assembly of pyridinearene to hexameric capsules
2019
Pyridinearene macrocycles have previously shown unique host–guest properties in their capsular dimers including endo complexation of neutral molecules and exo complexation of anions. Here, we demonstrate for the first time the formation of hydrogen bonded hexamer of tetraisobutyl-octahydroxypyridinearene in all three states of matter – gas phase, solution and solid-state. Cationic tris(bipyridine)ruthenium(II) template was found to stabilize the hexamer in gas phase, whereas solvent molecules do this in condensed phases. In solution, the capsular hexamer was found to be the thermodynamically favoured self-assembly product and transition from dimer to hexamer occurred in course of time. The …
Synthesis of 9,9′-Spirobifluorenes and 4,5-Diaza-9,9′-spirobifluorenes and Their Application as Affinity Materials for Quartz Crystal Microbalances
2017
Two different classes of aza analogues of 9,9'-spirobifluorenes have been synthesized. These were obtained by either furnishing the spirobifluorene with additional pyridyl moieties or by installing the aza function directly into the spirobifluorene core. These structurally rigid compounds were then evaluated as affinity materials for quartz crystal microbalances and proved to be highly potent for the detection of volatile organic compounds.
Polymorphic chiral squaraine crystallites in textured thin films
2020
Chirality 32(5), 619 - 631 (2020). doi:10.1002/chir.23213
Resolution and Determination of the Absolute Configuration of a Twisted Bis-Lactam Analogue of Tröger's Base: A Comparative Spectroscopic and Computa…
2015
The first reported twisted bis-lactam, a racemic Tröger's base (TB) analogue (2), was resolved into its enantiomers on a chiral stationary phase HPLC column. The absolute configuration of (+)-2 was determined to be (R,R)-2 by comparing experimental and calculated vibrational circular dichroism (VCD) and electronic circular dichroism (ECD) spectra. The absolute configuration of (-)-2 was determined by comparing experimental and calculated electronic circular dichroism (ECD) spectra. The corresponding theoretical spectra were calculated using the lowest energy conformation of (R,R)-2 and (S,S)-2 at the B3LYP/6-31G(d,p) level of theory. The absolute configuration of (+)-2 was also determined t…
Chiral self-sorting behaviour of [2.2]paracyclophane-based bis(pyridine) ligands
2019
Two constitutionally isomeric chiral bis(pyridine) ligands based on planar chiral 4,15-difunctionalized [2.2]paracyclophanes were synthesized, the respective enantiomers were separated via HPLC on a chiral stationary phase, and their self-assembly behaviour upon coordination to palladium(ii) ions was studied with regard to chiral self-sorting effects. As proven by NMR spectroscopy, mass spectrometry, CD spectroscopy, UV-Vis spectroscopy and X-ray crystallography both ligands form the expected dinuclear complexes upon coordination to cis-protected di- or tetravalent palladium(ii) ions, respectively, however, with distinct differences concerning their chiral self-sorting ability. peerReviewed
Electron-deficient trifluoromethyl-substituted sub-components affect the properties of M4L4 tetrahedral cages
2017
Two supramolecular tetrahedral cages based on a new electron-deficient trifluoromethyl-substituted pyridylimine ligand are synthesised by sub-component self-assembly. Their structures are characterised by NMR und UV-Vis spectroscopy, high-resolution mass spectrometry and single crystal X-ray diffraction. The iron(II) complex shows host–guest chemistry, complex-to-complex transformations and novel electronic properties.
Influencing the Self‐Sorting Behavior of [2.2]Paracyclophane‐Based Ligands by Introducing Isostructural Binding Motifs
2020
Abstract Two isostructural ligands with either nitrile (Lnit) or isonitrile (Liso) moieties directly connected to a [2.2]paracyclophane backbone with pseudo‐meta substitution pattern have been synthesized. The ligand itself (Lnit) or its precursors (Liso) were resolved by HPLC on a chiral stationary phase and the absolute configuration of the isolated enantiomers was assigned by XRD analysis and/or by comparison of quantum‐chemical simulated and experimental electronic circular dichroism (ECD) spectra. Surprisingly, the resulting metallosupramolecular aggregates formed in solution upon coordination of [(dppp)Pd(OTf)2] differ in their composition: whereas Lnit forms dinuclear complexes, Liso…
Subcomponent self‐assembly of a cyclic tetranuclear Fe(II) helicate in a highly diastereoselective self‐sorting manner
2019
Abstract An enantiomerically pure diamine based on the 4,15‐difunctionalized [2.2]paracyclophane scaffold and 2‐formylpyridine self‐assemble into an optically pure cyclic metallosupramolecular Fe4L6 helicate upon mixing with iron(II) ions in a diastereoselective subcomponent self‐assembly process. The cyclic assembly results from steric strain that prevents the formation of a smaller linear dinuclear triple‐stranded helicate, and hence, leads to the larger strain‐free assembly that fulfils the maximum occupancy rule. Interestingly, use of the racemic diamine also leads to a racemic mixture of the homochiral cyclic helicates as the major product in a highly diastereoselective narcissistic ch…
Synthesis and Isolation of Enantiomerically Enriched Cyclopenta[b]benzofurans Based on Products from Anodic Oxidation of 2,4-Dimethylphenol
2015
The anodic treatment of 2,4-dimethylphenol offers a powerful and direct method for the construction of a dehydrotetramer with four contiguous stereocentres on a multigram scale. The installation of propellanes on this scaffold using enantiomerically pure carbonyl compounds leads to a mixture of diastereomers. This mixture is easily separable using standard chromatography and gives rise to optically pure cyclopenta[b]benzofurans which are important scaffolds in a variety of natural products. The synthesis is easy to perform and allows a reliable access to chiral compounds with very high enantiomeric excess. It was possible to determine the absolute configuration of these compounds by compari…
Chiroptical inversion of a planar chiral redox-switchable rotaxane.
2019
Reversible redox-switching of a planar chiral [2]rotaxane with a tetrathiafulvalene-bearing crown ether macrocycle generates a complete sign reversal of the main band in the ECD spectrum, as shown by experiment and rationalised by DFT calculations.
An Octanuclear Metallosupramolecular Cage Designed To Exhibit Spin-Crossover Behavior.
2018
By employing the subcomponent self-assembly approach utilizing 5,10,15,20-tetrakis(4-aminophenyl)porphyrin or its zinc(II) complex, 1H-4-imidazolecarbaldehyde, and either zinc(II) or iron(II) salts, we were able to prepare O-symmetric cages having a confined volume of ca. 1300 Å3 . The use of iron(II) salts yielded coordination cages in the high-spin state at room temperature, manifesting spin-crossover in solution at low temperatures, whereas corresponding zinc(II) salts led to the corresponding diamagnetic analogues. The new cages were characterized by synchrotron X-ray crystallography, high-resolution mass spectrometry, and NMR, Mössbauer, IR, and UV/Vis spectroscopy. The cage structures…
Ein enantiomerenreines metallosupramolekulares Pd4L8-Aggregat mit neuartigem Strukturmotiv: Bildung durch einen Anionen-Templateffekt
2014
Ein enantiomerenreiner Bis(3-pyridyl)-Ligand 1 auf der Basis eines BINOL-Gerusts bildet mit tetravalenten PdII-Ionen einen homochiralen [Pd4(1)8]-Komplex. Zwei Tetrafluoroborationen dienen dabei als Template fur die Bildung dieses Aggegates und werden in zwei periphere Kavitaten eingeschlossen. Die dadurch resultierende Struktur reprasentiert ein neues Strukturmotiv fur diese Sorte von metallosupramolekularen Assemblaten, in dem die vier Palladiumionen in einer verzerrt tetraedrischen Anordnung zu finden sind. Dies zwingt den Liganden 1, zwei verschiedene Konformationen in dem Aggregat einzunehmen. Beide Phanomene sind einzigartig und fuhren uberdies zur Bildung einer dreidimensionalen Stru…
Chiral Self-Sorting of trans-Chelating Chiral Ligands upon Formation of PdII Complexes
2014
Invited for the cover of this issue is the group of Arne Lutzen at the University of Bonn, Germany. The cover image shows two dissymmetric bis(3-pyridyl) ligands based on a planar chiral pseudo-ortho-disubstituted [2.2]paracyclophane scaffold. Upon forming a mononuclear [ML2] complex with palladium(II) ions, these ligands act in a trans-chelating manner and undergo complete chiral self-sorting.
Stepwise Construction of Heterobimetallic Cages by an Extended Molecular Library Approach.
2017
Two novel heterobimetallic complexes, a trigonal-bipyramidal and a cubic one, have been synthesized and characterized using the same C3-symmetric metalloligand, prepared by a simple subcomponent self-assembly strategy. Adopting the molecular library approach, we chose a mononuclear, preorganized iron(II) complex as the metalloligand capable of self-assembly into a trigonal-bipyramidal or a cubic aggregate upon coordination to cis-protected C2-symmetric palladium(II) or unprotected tetravalent palladium(II) ions, respectively. The trigonal-bipyramidal complex was characterized by NMR and UV–vis spectroscopy, electrospray ionization mass spectrometry (ESI-MS), and single-crystal X-ray diffrac…
Simultaneous endo and exo Complex Formation of Pyridine[4]arene Dimers with Neutral and Anionic Guests
2017
The formation of complexes between hexafluorophosphate (PF6- ) and tetraisobutyloctahydroxypyridine[4]arene has been thoroughly studied in the gas phase (ESI-QTOF-MS, IM-MS, DFT calculations), in the solid state (X-ray crystallography), and in chloroform solution (1 H, 19 F, and DOSY NMR spectroscopy). In all states of matter, simultaneous endo complexation of solvent molecules and exo complexation of a PF6- anion within a pyridine[4]arene dimer was observed. While similar ternary complexes are often observed in the solid state, this is a unique example of such behavior in the gas phase.
Simultaneous Endo- and Exo-Complex Formation of Pyridine[4]arene Dimer with Neutral and Anionic Guests
2017
The formation of complexes between hexafluorophosphate (PF6−) and tetraisobutyloctahydroxypyridine[4]arene has been thoroughly studied in the gas phase (ESI‐QTOF‐MS, IM‐MS, DFT calculations), in the solid state (X‐ray crystallography), and in chloroform solution (1H, 19F, and DOSY NMR spectroscopy). In all states of matter, simultaneous endo complexation of solvent molecules and exo complexation of a PF6− anion within a pyridine[4]arene dimer was observed. While similar ternary complexes are often observed in the solid state, this is a unique example of such behavior in the gas phase. peerReviewed
Electron-deficient trifluoromethyl-substituted sub-components affect the properties of M4L4 tetrahedral cages
2017
Two supramolecular tetrahedral cages based on a new electron-deficient trifluoromethyl-substituted pyridylimine ligand are synthesised by sub-component self-assembly. Their structures are characterised by NMR und UV-Vis spectroscopy, high-resolution mass spectrometry and single crystal X-ray diffraction. The iron(II) complex shows host–guest chemistry, complex-to-complex transformations and novel electronic properties. peerReviewed
Influencing the self‐sorting behavior of [2.2]paracyclophane based ligands by introducing isostructural binding motifs
2020
Two isostructural ligands with either nitrile ( L nit ) or isonitrile ( L iso ) moieties directly connected to a [2.2]paracyclophane backbone with pseudo‐meta substitution pattern have been synthesized. The ligand itself ( L nit ) or its precursors ( L iso ) were resolved via HPLC on a chiral stationary phase and the absolute configuration of the isolated enantiomers was assigned by XRD analysis and/or by comparison of quantum‐chemical simulated and experimental ECD‐spectra. Surprisingly, the resulting metallosupramolecular aggregates formed in solution upon coordination of [(dppp)Pd(OTf) 2 ] differ in their composition: whereas L nit forms dinuclear complexes L iso exclusively forms trinuc…
CCDC 1959607: Experimental Crystal Structure Determination
2020
Related Article: Jennifer Zablocki, Oriol Arteaga, Frank Balzer, Dirk Hertel, Julian J. Holstein, Guido Clever, Jana Anhäuser, Rakesh Puttreddy, Kari Rissanen, Klaus Meerholz, Arne Lützen, Manuela Schiek|2020|Chirality|32|619|doi:10.1002/chir.23213
CCDC 1910670: Experimental Crystal Structure Determination
2019
Related Article: Marius Gaedke, Felix Witte, Jana Anhäuser, Henrik Hupatz, Hendrik V. Schröder, Arto Valkonen, Kari Rissanen, Arne Lützen, Beate Paulus, Christoph A. Schalley |2019|Chemical Science|10|10003|doi:10.1039/C9SC03694F
CCDC 1543476: Experimental Crystal Structure Determination
2017
Related Article: Anniina Kiesilä, Lauri Kivijärvi, Ngong Kodiah Beyeh, Jani O. Moilanen, Michael Groessl, Tatiana Rothe, Sven Götz, Filip Topić, Kari Rissanen, Arne Lützen and Elina Kalenius|2017|Angew.Chem.,Int.Ed.|56|10942|doi:10.1002/anie.201704054
CCDC 986176: Experimental Crystal Structure Determination
2014
Related Article: Georg Meyer-Eppler, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Inorg.Chem.||2495|doi:10.1002/ejic.201402057
CCDC 1919439: Experimental Crystal Structure Determination
2019
Related Article: Jana Anhäuser, Rakesh Puttreddy, Lukas Glanz, Andreas Schneider, Marianne Engeser, Kari Rissanen, Arne Lützen|2019|Chem.-Eur.J.|25|12294|doi:10.1002/chem.201903164
CCDC 1047644: Experimental Crystal Structure Determination
2017
Related Article: Michael Mirion, Lars Andernach, Caroline Stobe, Joaquin Barjau, Dieter Schollmeyer, Till Opatz, Arne Lützen, Siegfried R. Waldvogel|2015|Eur.J.Org.Chem.|2015|4876|doi:10.1002/ejoc.201500600
CCDC 1573413: Experimental Crystal Structure Determination
2017
Related Article: Niklas Struch, Filip Topic, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2018|Inorg.Chem.|57|241|doi:10.1021/acs.inorgchem.7b02412
CCDC 1451726: Experimental Crystal Structure Determination
2017
Related Article: Niklas Struch, Christoph Bannwarth, Tanya K. Ronson, Yvonne Lorenz, Bernd Mienert, Norbert Wagner, Marianne Engeser, Eckhard Bill, Rakesh Puttreddy, Kari Rissanen, Johannes Beck, Stefan Grimme, Jonathan R. Nitschke, Arne Lützen|2017|Angew.Chem.,Int.Ed.|56|4930|doi:10.1002/anie.201700832
CCDC 986175: Experimental Crystal Structure Determination
2014
Related Article: Georg Meyer-Eppler, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Inorg.Chem.||2495|doi:10.1002/ejic.201402057
CCDC 1966422: Experimental Crystal Structure Determination
2020
Related Article: Jennifer Zablocki, Oriol Arteaga, Frank Balzer, Dirk Hertel, Julian J. Holstein, Guido Clever, Jana Anhäuser, Rakesh Puttreddy, Kari Rissanen, Klaus Meerholz, Arne Lützen, Manuela Schiek|2020|Chirality|32|619|doi:10.1002/chir.23213
CCDC 1047645: Experimental Crystal Structure Determination
2017
Related Article: Michael Mirion, Lars Andernach, Caroline Stobe, Joaquin Barjau, Dieter Schollmeyer, Till Opatz, Arne Lützen, Siegfried R. Waldvogel|2015|Eur.J.Org.Chem.|2015|4876|doi:10.1002/ejoc.201500600
CCDC 945021: Experimental Crystal Structure Determination
2013
Related Article: Christoph Gütz, Rainer Hovorka, Caroline Stobe, Niklas Struch, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Org.Chem.|2014|206|doi:10.1002/ejoc.201301314
CCDC 1573412: Experimental Crystal Structure Determination
2017
Related Article: Niklas Struch, Filip Topic, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2018|Inorg.Chem.|57|241|doi:10.1021/acs.inorgchem.7b02412
CCDC 1573312: Experimental Crystal Structure Determination
2017
Related Article: Niklas Struch, Filip Topic, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2018|Inorg.Chem.|57|241|doi:10.1021/acs.inorgchem.7b02412
CCDC 1824417: Experimental Crystal Structure Determination
2020
Related Article: Lucia Volbach, Niklas Struch, Fabian Bohle, Filip Topić, Gregor Schnakenburg, Andreas Schneider, Kari Rissanen, Stefan Grimme, Arne Lützen|2020|Chem.-Eur.J.|26|3335|doi:10.1002/chem.201905070
CCDC 1824416: Experimental Crystal Structure Determination
2020
Related Article: Lucia Volbach, Niklas Struch, Fabian Bohle, Filip Topić, Gregor Schnakenburg, Andreas Schneider, Kari Rissanen, Stefan Grimme, Arne Lützen|2020|Chem.-Eur.J.|26|3335|doi:10.1002/chem.201905070
CCDC 1955599: Experimental Crystal Structure Determination
2020
Related Article: Lucia Volbach, Niklas Struch, Fabian Bohle, Filip Topić, Gregor Schnakenburg, Andreas Schneider, Kari Rissanen, Stefan Grimme, Arne Lützen|2020|Chem.-Eur.J.|26|3335|doi:10.1002/chem.201905070
CCDC 945019: Experimental Crystal Structure Determination
2013
Related Article: Christoph Gütz, Rainer Hovorka, Caroline Stobe, Niklas Struch, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Org.Chem.|2014|206|doi:10.1002/ejoc.201301314
CCDC 1573313: Experimental Crystal Structure Determination
2017
Related Article: Niklas Struch, Filip Topic, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2018|Inorg.Chem.|57|241|doi:10.1021/acs.inorgchem.7b02412
CCDC 986177: Experimental Crystal Structure Determination
2014
Related Article: Georg Meyer-Eppler, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Inorg.Chem.||2495|doi:10.1002/ejic.201402057
CCDC 1919442: Experimental Crystal Structure Determination
2019
Related Article: Jana Anhäuser, Rakesh Puttreddy, Lukas Glanz, Andreas Schneider, Marianne Engeser, Kari Rissanen, Arne Lützen|2019|Chem.-Eur.J.|25|12294|doi:10.1002/chem.201903164
CCDC 1550913: Experimental Crystal Structure Determination
2017
Related Article: Matthias Hardy, Niklas Struch, Filip Topic, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2018|Inorg.Chem.|57|3507|doi:10.1021/acs.inorgchem.7b02516
CCDC 1573410: Experimental Crystal Structure Determination
2017
Related Article: Niklas Struch, Filip Topic, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2018|Inorg.Chem.|57|241|doi:10.1021/acs.inorgchem.7b02412
CCDC 1003004: Experimental Crystal Structure Determination
2014
Related Article: Christoph Gütz , Rainer Hovorka , Niklas Struch , Jens Bunzen , Georg Meyer-Eppler , Zheng-Wang Qu , Stefan Grimme , Filip Topić, Kari Rissanen, Mario Cetina, Marianne Engeser, Arne Lützen|2014|J.Am.Chem.Soc.|136|11830|doi:10.1021/ja506327c
CCDC 1919441: Experimental Crystal Structure Determination
2019
Related Article: Jana Anhäuser, Rakesh Puttreddy, Lukas Glanz, Andreas Schneider, Marianne Engeser, Kari Rissanen, Arne Lützen|2019|Chem.-Eur.J.|25|12294|doi:10.1002/chem.201903164
CCDC 999739: Experimental Crystal Structure Determination
2014
Related Article: Rainer Hovorka, Georg Meyer-Eppler, Torsten Piehler, Sophie Hytteballe, Marianne Engeser, Filip Topić, Kari Rissanen, Arne Lützen|2014|Chem.-Eur.J.|20|13253|doi:10.1002/chem.201403414
CCDC 1919440: Experimental Crystal Structure Determination
2019
Related Article: Jana Anhäuser, Rakesh Puttreddy, Lukas Glanz, Andreas Schneider, Marianne Engeser, Kari Rissanen, Arne Lützen|2019|Chem.-Eur.J.|25|12294|doi:10.1002/chem.201903164
CCDC 1047647: Experimental Crystal Structure Determination
2017
Related Article: Michael Mirion, Lars Andernach, Caroline Stobe, Joaquin Barjau, Dieter Schollmeyer, Till Opatz, Arne Lützen, Siegfried R. Waldvogel|2015|Eur.J.Org.Chem.|2015|4876|doi:10.1002/ejoc.201500600
CCDC 986178: Experimental Crystal Structure Determination
2014
Related Article: Georg Meyer-Eppler, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Inorg.Chem.||2495|doi:10.1002/ejic.201402057
CCDC 1573414: Experimental Crystal Structure Determination
2017
Related Article: Niklas Struch, Filip Topic, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2018|Inorg.Chem.|57|241|doi:10.1021/acs.inorgchem.7b02412
CCDC 971933: Experimental Crystal Structure Determination
2015
Related Article: Rainer Hovorka, Sophie Hytteballe, Torsten Piehler, Georg Meyer-Eppler, Filip Topić, Kari Rissanen, Marianne Engeser, Arne Lützen|2014|Beilstein J.Org.Chem.|10|432|doi:10.3762/bjoc.10.40
CCDC 1899745: Experimental Crystal Structure Determination
2019
Related Article: Anniina Kiesilä, Ngong Kodiah Beyeh, Jani O. Moilanen, Rakesh Puttreddy, Sven Götz, Kari Rissanen, Perdita Barran, Arne Lützen, Elina Kalenius|2019|Org.Biomol.Chem.|17|6980|doi:10.1039/C9OB01383K
CCDC 941094: Experimental Crystal Structure Determination
2013
Related Article: Christoph Gütz, Rainer Hovorka, Caroline Stobe, Niklas Struch, Filip Topić, Gregor Schnakenburg, Kari Rissanen, Arne Lützen|2014|Eur.J.Org.Chem.|2014|206|doi:10.1002/ejoc.201301314
CCDC 945020: Experimental Crystal Structure Determination
2013
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CCDC 1037524: Experimental Crystal Structure Determination
2015
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CCDC 941095: Experimental Crystal Structure Determination
2013
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CCDC 1955601: Experimental Crystal Structure Determination
2020
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CCDC 1575238: Experimental Crystal Structure Determination
2017
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CCDC 1573411: Experimental Crystal Structure Determination
2017
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CCDC 982088: Experimental Crystal Structure Determination
2014
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CCDC 1047646: Experimental Crystal Structure Determination
2017
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CCDC 1955600: Experimental Crystal Structure Determination
2020
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