@article{41003,
abstract = {{Combining strong σ-donating N-heterocyclic carbene ligands and π-accepting pyridine ligands with a high octahedricity in rigid iron(II) complexes increases the 3MLCT lifetime from 0.15 ps in the prototypical [Fe(tpy)2]2+ complex to 9.2 ps in [Fe(dpmi)2]2+12+. The tripodal CNN ligand dpmi (di(pyridine-2-yl)(3-methylimidazol-2-yl)methane) forms six-membered chelate rings with the iron(II) centre leading to close to 90° bite angles and enhanced iron-ligand orbital overlap}},
author = {{Reuter, Thomas and Kruse, Ayla and Schoch, Roland and Lochbrunner, Stefan and Bauer, Matthias and Heinze, Katja}},
issn = {{1359-7345}},
journal = {{Chemical Communications}},
keywords = {{Materials Chemistry, Metals and Alloys, Surfaces, Coatings and Films, General Chemistry, Ceramics and Composites, Electronic, Optical and Magnetic Materials, Catalysis}},
number = {{61}},
pages = {{7541--7544}},
publisher = {{Royal Society of Chemistry (RSC)}},
title = {{{Higher MLCT lifetime of carbene iron(ii) complexes by chelate ring expansion}}},
doi = {{10.1039/d1cc02173g}},
volume = {{57}},
year = {{2021}},
}
@article{40997,
abstract = {{On transition metals such as iron rests lots of hope to replace precious metal catalysts in the field of photochemistry for a more sustainable future. Indeed, significant progress has been made in recent years in terms of lifetime extension and emerging applications in catalysis. For this reason, recent synthetic strategies of new photoactive iron compounds, which have proved to show particularly promising properties, are reviewed here. The lifetime of the excited state serves as a key parameter for comparison with the standard ruthenium complex, [Ru(bpy)3]2+, to discuss the potential and performance of the iron complexes. This approach is complemented by a more holistic examination of the sustainability of such a substitution strategy in order to answer the question: when or at which point can we assume that iron represents a more sustainable alternative for noble metals in photochemical applications?}},
author = {{Dierks, Philipp and Vukadinovic, Yannik and Bauer, Matthias}},
issn = {{2052-1553}},
journal = {{Inorganic Chemistry Frontiers}},
keywords = {{Inorganic Chemistry}},
number = {{2}},
pages = {{206--220}},
publisher = {{Royal Society of Chemistry (RSC)}},
title = {{{Photoactive iron complexes: more sustainable, but still a challenge}}},
doi = {{10.1039/d1qi01112j}},
volume = {{9}},
year = {{2021}},
}
@article{41000,
abstract = {{Metal-catalyzed C−H activations are environmentally and economically attractive synthetic strategies for the construction of functional molecules as they obviate the need for pre-functionalized substrates and minimize waste generation. Great challenges reside in the control of selectivities, the utilization of unbiased hydrocarbons, and the operation of atom-economical dehydrocoupling mechanisms. An especially mild borylation of benzylic CH bonds was developed with the ligand-free pre-catalyst Co[N(SiMe3)2]2 and the bench-stable and inexpensive borylation reagent B2pin2 that produces H2 as the only by-product. A full set of kinetic, spectroscopic, and preparative mechanistic studies are indicative of a tandem catalysis mechanism of CH-borylation and dehydrocoupling via molecular CoI catalysts.}},
author = {{Ghosh, Pradip and Schoch, Roland and Bauer, Matthias and Jacobi von Wangelin, Axel}},
issn = {{1433-7851}},
journal = {{Angewandte Chemie International Edition}},
keywords = {{General Chemistry, Catalysis}},
number = {{1}},
publisher = {{Wiley}},
title = {{{Selective Benzylic CH‐Borylations by Tandem Cobalt Catalysis}}},
doi = {{10.1002/anie.202110821}},
volume = {{61}},
year = {{2021}},
}
@article{41013,
abstract = {{Within this article, it is shown that an electrochemical defluorination and additional fluorination of Ruddlesden–Popper-type La2NiO3F2 is possible within all-solid-state fluoride-ion batteries. Structural changes within the reduced and oxidized phases have been examined by X-ray diffraction studies at different states of charging and discharging. The synthesis of the oxidized phase La2NiO3F2+x proved to be successful by structural analysis using both X-ray powder diffraction and automated electron diffraction tomography techniques. The structural reversibility on re-fluorinating and re-defluorinating is also demonstrated. Moreover, the influence of different sequences of consecutive reduction and oxidation steps on the formed phases has been investigated. The observed structural changes have been compared to changes in phases obtained via other topochemical modification approaches such as hydride-based reduction and oxidative fluorination using F2 gas, highlighting the potential of such electrochemical reactions as alternative synthesis routes. Furthermore, the electrochemical routes represent safe and controllable synthesis approaches for novel phases, which cannot be synthesized via other topochemical methods. Additionally, side reactions, occurring alongside the desired electrochemical reactions, have been addressed and the cycling performance has been studied.}},
author = {{Wissel, Kerstin and Schoch, Roland and Vogel, Tobias and Donzelli, Manuel and Matveeva, Galina and Kolb, Ute and Bauer, Matthias and Slater, Peter R. and Clemens, Oliver}},
issn = {{0897-4756}},
journal = {{Chemistry of Materials}},
keywords = {{Materials Chemistry, General Chemical Engineering, General Chemistry}},
number = {{2}},
pages = {{499--512}},
publisher = {{American Chemical Society (ACS)}},
title = {{{Electrochemical Reduction and Oxidation of Ruddlesden–Popper-Type La2NiO3F2 within Fluoride-Ion Batteries}}},
doi = {{10.1021/acs.chemmater.0c01762}},
volume = {{33}},
year = {{2021}},
}
@article{41010,
abstract = {{We present the η3-coordination of the 2-phosphaethynthiolate anion in the complex (PN)2La(SCP) (2) [PN=N-(2-(diisopropylphosphanyl)-4-methylphenyl)-2,4,6-trimethylanilide)]. Structural comparison with dinuclear thiocyanate-bridged (PN)2La(μ-1,3-SCN)2La(PN)2 (3) and azide-bridged (PN)2La(μ-1,3-N3)2La(PN)2 (4) complexes indicates that the [SCP]− coordination mode is mainly governed by electronic, rather than steric factors. Quantum mechanical investigations reveal large contributions of the antibonding π*-orbital of the [SCP]− ligand to the LUMO of complex 2, rendering it the ideal precursor for the first functionalization of the [SCP]− anion. Complex 2 was therefore reacted with CAACs which induced a selective rearrangement of the [SCP]− ligand to form the first CAAC stabilized group 15–group 16 fulminate-type complexes (PN)2La{SPC(RCAAC)} (5 a,b, R=Ad, Me). A detailed reaction mechanism for the SCP-to-SPC isomerization is proposed based on DFT calculations.}},
author = {{Watt, Fabian A. and Burkhardt, Lukas and Schoch, Roland and Mitzinger, Stefan and Bauer, Matthias and Weigend, Florian and Goicoechea, Jose M. and Tambornino, Frank and Hohloch, Stephan}},
issn = {{1433-7851}},
journal = {{Angewandte Chemie International Edition}},
keywords = {{General Chemistry, Catalysis}},
number = {{17}},
pages = {{9534--9539}},
publisher = {{Wiley}},
title = {{{η 3 ‐Coordination and Functionalization of the 2‐Phosphaethynthiolate Anion at Lanthanum(III)**}}},
doi = {{10.1002/anie.202100559}},
volume = {{60}},
year = {{2021}},
}
@article{41012,
abstract = {{Here we explore the electronic structure of the diiron complex [(dppf)Fe(CO)3]0/+ [10/+; dppf = 1,1′-bis(diphenylphosphino)ferrocene] in two oxidation states by an advanced multitechnique experimental approach. A combination of magnetic circular dichroism, X-ray absorption and emission, high-frequency electron paramagnetic resonance (EPR), and Mössbauer spectroscopies is used to establish that oxidation of 10 occurs on the carbonyl iron ion, resulting in a low-spin iron(I) ion. It is shown that an unequivocal result is obtained by combining several methods. Compound 1+ displays slow spin dynamics, which is used here to study its geometric structure by means of pulsed EPR methods. Surprisingly, these data show an association of the tetrakis[3,5-bis(trifluoromethylphenyl)]borate counterion with 1+.}},
author = {{Winkler, Mario and Schnierle, Marc and Ehrlich, Felix and Mehnert, Kim-Isabelle and Hunger, David and Sheveleva, Alena M. and Burkhardt, Lukas and Bauer, Matthias and Tuna, Floriana and Ringenberg, Mark R. and van Slageren, Joris}},
issn = {{0020-1669}},
journal = {{Inorganic Chemistry}},
keywords = {{Inorganic Chemistry, Physical and Theoretical Chemistry}},
number = {{5}},
pages = {{2856--2865}},
publisher = {{American Chemical Society (ACS)}},
title = {{{Electronic Structure of a Diiron Complex: A Multitechnique Experimental Study of [(dppf)Fe(CO) 3]+/0}}},
doi = {{10.1021/acs.inorgchem.0c03259}},
volume = {{60}},
year = {{2021}},
}
@article{41011,
abstract = {{The controlled assembly of well-defined planar nanoclusters from molecular precursors is synthetically challenging and often plagued by the predominant formation of 3D-structures and nanoparticles. Herein, we report planar iron hydride nanoclusters from reactions of main group element hydrides with iron(II) bis(hexamethyldisilazide). The structures and properties of isolated Fe4, Fe6, and Fe7 nanoplatelets and calculated intermediates enable an unprecedented insight into the underlying building principle and growth mechanism of iron clusters, metal monolayers, and nanoparticles.}},
author = {{Chakraborty, Uttam and Bügel, Patrick and Fritsch, Lorena and Weigend, Florian and Bauer, Matthias and Jacobi von Wangelin, Axel}},
issn = {{2191-1363}},
journal = {{ChemistryOpen}},
keywords = {{General Chemistry}},
number = {{2}},
pages = {{265--271}},
publisher = {{Wiley}},
title = {{{Planar Iron Hydride Nanoclusters: Combined Spectroscopic and Theoretical Insights into Structures and Building Principles}}},
doi = {{10.1002/open.202000307}},
volume = {{10}},
year = {{2021}},
}
@article{25894,
abstract = {{Powder X-ray diffraction (XRD) patterns of ordered mesoporous CMK-8 and CMK-9 carbon materials are simulated by geometric modeling. The materials are amorphous at the atomic length scale but exhibit highly symmetric gyroidal structures at the nanometer scale, corresponding to regular, continuous nanopore systems with cubic symmetry. Their structures lead to characteristic low-angle XRD signatures. We introduce a model based on geometrical considerations to simulate CMK-8 and CMK-9 structures with variable volume fraction of carbon (vs. pore volume, i.e., variable 'pore wall thickness'). In addition, we also simulate carbon materials with variable amounts of guest species (e.g., sulfur) residing in their pores. The corresponding XRD patterns are calculated. The carbon volume fraction turns out to have a significant impact on the relative diffraction peak intensities, especially in case of CMK-9 carbon that features a bimodal porosity. Likewise, the presence of guest species in the pores may also strongly affect the relative peak intensities. Our study suggests that careful evaluation of experimental low-angle XRD patterns of (real) CMK-8 or CMK-9 materials offers an opportunity to obtain detailed information about the nanostructural properties in addition to the mere identification of the pore systems geometry.}},
author = {{Schwind, Bertram and Smått, Jan-Henrik and Tiemann, Michael and Weinberger, Christian}},
issn = {{1387-1811}},
journal = {{Microporous and Mesoporous Materials}},
title = {{{Modeling of gyroidal mesoporous CMK-8 and CMK-9 carbon nanostructures and their X-Ray diffraction patterns}}},
doi = {{10.1016/j.micromeso.2020.110330}},
year = {{2021}},
}
@article{25897,
abstract = {{A comparison of infrared spectroscopic analytical approaches was made in order to assess their applicability for internal structure characterization of SiO2 thin films. Markers for porosity and/or disorder based on the analysis of the asymmetric stretching absorption band of SiO2 between 900−1350 cm−1 were discussed. The shape of this band, which shows a well-defined LO–TO splitting, depends not only on the inherent characteristics of the film under analysis but also on the particular geometry of the IR experiment and the specific surface selection rules of the substrate. Three types of SiO2 thin films with clearly defined porosity ranging from dense films to mesoporous films were investigated by transmission (at different incidence angles), direct specular reflection (at different angles), and diffuse reflection. Two different types of substrate, metallic and semiconducting, were used. The combined effect of substrate and specific technique in the final shape of the band, was discussed, and the efficacy for their applicability to the determination of porosity in thin SiO2 films was critically evaluated.}},
author = {{de los Arcos, Teresa and Müller, Hendrik and Wang, Fuzeng and Damerla, Varun Raj and Hoppe, Christian and Weinberger, Christian and Tiemann, Michael and Grundmeier, Guido}},
issn = {{0924-2031}},
journal = {{Vibrational Spectroscopy}},
title = {{{Review of infrared spectroscopy techniques for the determination of internal structure in thin SiO2 films}}},
doi = {{10.1016/j.vibspec.2021.103256}},
year = {{2021}},
}
@article{25893,
abstract = {{Tailor-made ordered mesoporous materials bear great potential in numerous fields of application where large interfaces are required. However, the inherent surfacechemical properties of conventional materials, such as silica, carbon or organosilica, poses some limitations with respect to their application. Surface manipulation by functionalization with chemically more reactive groups is one way to improve materials for their desired purpose. Another approach is the design of high surface-area composite materials. The surface manipulation, either by functionalization or by introducing guest species, can be performed selectively. This means that when several distinct, i.e. , hierarchical, types of surfaces or pore systems exist in a material, each of them may be chosen for manipulation. Several strategies can be identified to achieve this goal. Molecules or molecule assemblies can be utilized to temporarily protect pores or surfaces (soft protection), while manipulation occurs at the accessible sites. This approach is a recurring motive in this review and can also be applied to rigid template matrices (hard protection). Furthermore, the size of functionalization agents (size protection) and their reactivity/diffusion (kinetic protection) into the pores can also be utilized to achieve selectivity. In addition, challenges in the synthesis and characterization of selectively manipulated ordered mesoporous materials are discussed.}},
author = {{Tiemann, Michael and Weinberger, Christian}},
issn = {{2196-7350}},
journal = {{Advanced Materials Interfaces}},
title = {{{Selective Modification of Hierarchical Pores and Surfaces in Nanoporous Materials}}},
doi = {{10.1002/admi.202001153}},
year = {{2021}},
}
@article{25896,
abstract = {{In this report, a flame spray pyrolysis setup has been examined with various in situ extraction methods of particle samples along the flame axis. First, two precursor formulations leading to the formation of iron oxide nanoparticles were used in a standardized SpraySyn burner system, and the final particle outcome was characterized by a broad range of established powder characterization techniques (TEM/HRTEM, SAXS, XRD, BET). The characterization of the powder products evidenced that mostly homogeneous gas-to-particle conversion takes place when applying an acidic precursor solution, whereas the absence of the acid leads to a dominant droplet-to-particle pathway. Our study indicates that a droplet-to-particle-pathway could be present even when processing the acidic formulation. However, even if a secondary pathway might take place in this case as well, it is not dominant and nearly negligible. Subsequently, the in situ particle structure evolution was investigated for the dominant gas-to-particle pathway, and particles were extracted along the flame axis for online SMPS and offline TEM/HRTEM analysis. Due to the highly reactive conditions within the flame (high temperatures, turbulent flow field, high particle number concentrations), the extraction of representative samples from spray flames is challenging. In order to handle the reactive conditions, two extraction techniques were tailored in this report. To extract an aerosol sample within the flame for SMPS measurement, a Hole in a Tube probe was adjusted. Thus, the mobility particle diameter as well as the corresponding distribution widths were obtained at different heights above the burner along the flame axis. For TEM/HRTEM image analysis, particle samples were collected thermophoretically by means of a tailored shutter system. Since all sampling grids were protected until reaching the flame axis and due to the low sampling time, momentary captures of local particle structures could be extracted precisely. The particle morphologies have clearly shown an evolution from spherical and paired particles in the flame center to fractal and compact agglomerates at later synthesis stages.}},
author = {{Tischendorf, R. and Simmler, M. and Weinberger, Christian and Bieber, M. and Reddemann, M. and Fröde, F. and Lindner, J. and Pitsch, H. and Kneer, R. and Tiemann, Michael and Nirschl, H. and Schmid, H.-J.}},
issn = {{0021-8502}},
journal = {{Journal of Aerosol Science}},
title = {{{Examination of the evolution of iron oxide nanoparticles in flame spray pyrolysis by tailored in situ particle sampling techniques}}},
doi = {{10.1016/j.jaerosci.2020.105722}},
year = {{2021}},
}
@article{22635,
abstract = {{Photodynamic therapy (PDT) using TiO2 nanoparticles has become an important alternative treatment for different types of cancer due to their high photocatalytic activity and high absorption of UV-A light. To potentiate this treatment, we have coated commercial glass plates with TiO2 nanoparticles prepared by the sol–gel method (TiO2-m), which exhibit a remarkable selectivity for the irreversible trapping of cancer cells. The physicochemical properties of the deposited TiO2-m nanoparticle coatings have been characterized by a number of complementary surface-analytical techniques and their interaction with leukemia and healthy blood cells were investigated. Scanning electron and atomic force microscopy verify the formation of a compact layer of TiO2-m nanoparticles. The particles are predominantly in the anatase phase and have hydroxyl-terminated surfaces as revealed by Raman, X-ray photoelectron, and infrared spectroscopy, as well as X-ray diffraction. We find that lymphoblastic leukemia cells adhere to the TiO2-m coating and undergo amoeboid-like migration, whereas lymphocytic cells show distinctly weaker interactions with the coating. This evidences the potential of this nanomaterial coating to selectively trap cancer cells and renders it a promising candidate for the development of future prototypes of PDT devices for the treatment of leukemia and other types of cancers with non-adherent cells.}},
author = {{Garcia Diosa, Jaime Andres and Gonzalez Orive, Alejandro and Weinberger, Christian and Schwiderek, Sabrina and Knust, Steffen and Tiemann, Michael and Grundmeier, Guido and Keller, Adrian and Camargo Amado, Ruben Jesus}},
issn = {{1552-4973}},
journal = {{Journal of Biomedical Materials Research Part B: Applied Biomaterials}},
pages = {{2142–2153}},
title = {{{TiO2 nanoparticle coatings on glass surfaces for the selective trapping of leukemia cells from peripheral blood}}},
doi = {{10.1002/jbm.b.34862}},
volume = {{109}},
year = {{2021}},
}
@article{25892,
abstract = {{The tetratopic linker 1,1,2,2-tetrakis(4-phosphonophenyl)ethylene (H8TPPE) was used to synthesize the three new porous metal–organic frameworks of composition [M2(H2O)2(H2TPPE)]·xH2O (M = Al3+, Ga3+, Fe3+), denoted as M-CAU-53 under hydrothermal reaction conditions, using the corresponding metal nitrates as starting materials. The crystal structures of the compounds were determined ab initio from powder X-ray diffraction data, revealing small structural differences. Proton conductivity measurements were carried out, indicating different conductivity mechanisms. The differences in proton conductivity could be linked to the individual structures. In addition, a thorough characterization via thermogravimetry, elemental analysis, IR-spectroscopy as well as N2- and H2O-sorption is given.}},
author = {{Steinke, Felix and Javed, Ali and Wöhlbrandt, Stephan and Tiemann, Michael and Stock, Norbert}},
issn = {{1477-9226}},
journal = {{Dalton Transactions}},
pages = {{13572--13579}},
title = {{{New isoreticular phosphonate MOFs based on a tetratopic linker}}},
doi = {{10.1039/d1dt02610k}},
year = {{2021}},
}
@article{41007,
abstract = {{Two closely related FeII complexes with 2,6-bis(1-ethyl-1H-1,2,3-triazol-4yl)pyridine and 2,6-bis(1,2,3-triazol-5-ylidene)pyridine ligands are presented to gain new insights into the photophysics of bis(tridentate) iron(II) complexes. The [Fe(N^N^N)2]2+ pseudoisomer sensitizes singlet oxygen through a MC state with nanosecond lifetime after MLCT excitation, while the bis(tridentate) [Fe(C^N^C)2]2+ pseudoisomer possesses a similar 3MLCT lifetime as the tris(bidentate) [Fe(C^C)2(N^N)]2+ complexes with four mesoionic carbenes.}},
author = {{Dierks, Philipp and Kruse, Ayla and Bokareva, Olga S. and Al-Marri, Mohammed J. and Kalmbach, Jens and Baltrun, Marc and Neuba, Adam and Schoch, Roland and Hohloch, Stephan and Heinze, Katja and Seitz, Michael and Kühn, Oliver and Lochbrunner, Stefan and Bauer, Matthias}},
issn = {{1359-7345}},
journal = {{Chemical Communications}},
keywords = {{Materials Chemistry, Metals and Alloys, Surfaces, Coatings and Films, General Chemistry, Ceramics and Composite, Metallkomplexe, Optical and Magnetic Materials, Catalysis}},
number = {{54}},
pages = {{6640--6643}},
publisher = {{Royal Society of Chemistry (RSC)}},
title = {{{Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes}}},
doi = {{10.1039/d1cc01716k}},
volume = {{57}},
year = {{2021}},
}
@article{18534,
author = {{Vukadinovic, Yannik and Burkhardt, Lukas and Päpcke, Ayla and Miletic, Anabel and Fritsch, Lorena and Altenburger, Björn and Schoch, Roland and Neuba, Adam and Lochbrunner, Stefan and Bauer, Matthias}},
issn = {{0020-1669}},
journal = {{Inorganic Chemistry}},
pages = {{8762--8774}},
title = {{{When Donors Turn into Acceptors: Ground and Excited State Properties of FeII Complexes with Amine-Substituted Tridentate Bis-imidazole-2-ylidene Pyridine Ligands}}},
doi = {{10.1021/acs.inorgchem.0c00393}},
year = {{2020}},
}
@article{41022,
author = {{Kirchhof, Manuel and Gugeler, Katrin and Fischer, Felix Richard and Nowakowski, Michał and Bauer, Alina and Alvarez-Barcia, Sonia and Abitaev, Karina and Schnierle, Marc and Qawasmi, Yaseen and Frey, Wolfgang and Baro, Angelika and Estes, Deven P. and Sottmann, Thomas and Ringenberg, Mark R. and Plietker, Bernd and Bauer, Matthias and Kästner, Johannes and Laschat, Sabine}},
issn = {{0276-7333}},
journal = {{Organometallics}},
keywords = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry}},
number = {{17}},
pages = {{3131--3145}},
publisher = {{American Chemical Society (ACS)}},
title = {{{Experimental and Theoretical Study on the Role of Monomeric vs Dimeric Rhodium Oxazolidinone Norbornadiene Complexes in Catalytic Asymmetric 1,2- and 1,4-Additions}}},
doi = {{10.1021/acs.organomet.0c00310}},
volume = {{39}},
year = {{2020}},
}
@article{41015,
author = {{Benedikter, Mathis and Musso, Janis and Kesharwani, Manoj K. and Sterz, K. Leonard and Elser, Iris and Ziegler, Felix and Fischer, Felix and Plietker, Bernd and Frey, Wolfgang and Kästner, Johannes and Winkler, Mario and van Slageren, Joris and Nowakowski, Michał and Bauer, Matthias and Buchmeiser, Michael R.}},
issn = {{2155-5435}},
journal = {{ACS Catalysis}},
keywords = {{Catalysis, General Chemistry}},
number = {{24}},
pages = {{14810--14823}},
publisher = {{American Chemical Society (ACS)}},
title = {{{Charge Distribution in Cationic Molybdenum Imido Alkylidene N-Heterocyclic Carbene Complexes: A Combined X-ray, XAS, XES, DFT, Mössbauer, and Catalysis Approach}}},
doi = {{10.1021/acscatal.0c03978}},
volume = {{10}},
year = {{2020}},
}
@article{41020,
author = {{Gregori, Bernhard J. and Nowakowski, Michał and Schoch, Anke and Pöllath, Simon and Zweck, Josef and Bauer, Matthias and Jacobi von Wangelin, Axel}},
issn = {{1867-3880}},
journal = {{ChemCatChem}},
keywords = {{Inorganic Chemistry, Organic Chemistry, Physical and Theoretical Chemistry, Catalysis}},
number = {{21}},
pages = {{5359--5363}},
publisher = {{Wiley}},
title = {{{Stereoselective Chromium‐Catalyzed Semi‐Hydrogenation of Alkynes}}},
doi = {{10.1002/cctc.202000994}},
volume = {{12}},
year = {{2020}},
}
@article{16311,
author = {{Burkhardt, Lukas and Vukadinovic, Yannik and Nowakowski, Michał and Kalinko, Aleksandr and Rudolph, Julian and Carlsson, Per-Anders and Jacob, Christoph R. and Bauer, Matthias}},
issn = {{0020-1669}},
journal = {{Inorganic Chemistry}},
pages = {{3551--3561}},
title = {{{Electronic Structure of the Hieber Anion [Fe(CO)3(NO)]− Revisited by X-ray Emission and Absorption Spectroscopy}}},
doi = {{10.1021/acs.inorgchem.9b02092}},
year = {{2020}},
}
@phdthesis{41005,
author = {{Vukadinovic, Yannik}},
title = {{{N-heterocyclic carbene based iron and ruthenium photosensitizer with amine donors - A systematic study on spectroscopic differences}}},
doi = {{10.17619/UNIPB/1-1060}},
year = {{2020}},
}