@article{ZuAmsalemEggeretal.2019, author = {Zu, Fengshuo and Amsalem, Patrick and Egger, David A. and Wang, Rongbin and Wolff, Christian Michael and Fang, Honghua and Loi, Maria Antonietta and Neher, Dieter and Kronik, Leeor and Duhm, Steffen and Koch, Norbert}, title = {Constructing the Electronic Structure of CH3NH3PbI3 and CH3NH3PbBr3 Perovskite Thin Films from Single-Crystal Band Structure Measurements}, series = {The journal of physical chemistry letters}, volume = {10}, journal = {The journal of physical chemistry letters}, number = {3}, publisher = {American Chemical Society}, address = {Washington}, issn = {1948-7185}, doi = {10.1021/acs.jpclett.8b03728}, pages = {601 -- 609}, year = {2019}, abstract = {Photovoltaic cells based on halide perovskites, possessing remarkably high power conversion efficiencies have been reported. To push the development of such devices further, a comprehensive and reliable understanding of their electronic properties is essential but presently not available. To provide a solid foundation for understanding the electronic properties of polycrystalline thin films, we employ single-crystal band structure data from angle-resolved photoemission measurements. For two prototypical perovskites (CH3NH3PbBr3 and CH3NH3PbI3), we reveal the band dispersion in two high-symmetry directions and identify the global valence band maxima. With these benchmark data, we construct "standard" photoemission spectra from polycrystalline thin film samples and resolve challenges discussed in the literature for determining the valence band onset with high reliability. Within the framework laid out here, the consistency of relating the energy level alignment in perovskite-based photovoltaic and optoelectronic devices with their functional parameters is substantially enhanced.}, language = {en} } @article{ZucchiCorniaBoeseetal.1999, author = {Zucchi, Claudia and Cornia, Andrea and Boese, Roland and Kleinpeter, Erich and Alper, Howard and Palyi, Gyula}, title = {Preparation and molecular structures of benzyl- and phenyl-acetycobalt-carbonyls}, year = {1999}, language = {en} } @article{ZudeHashimHassetal.2019, author = {Zude, Manuela and Hashim, Norhashila and Hass, Roland and Polley, Nabarun and Regen, Christian}, title = {Validation study for measuring absorption and reduced scattering coefficients by means of laser-induced backscattering imaging}, series = {Postharvest Biology and Technology}, volume = {153}, journal = {Postharvest Biology and Technology}, publisher = {Elsevier}, address = {Amsterdam}, issn = {0925-5214}, doi = {10.1016/j.postharvbio.2019.04.002}, pages = {161 -- 168}, year = {2019}, abstract = {Decoupling of optical properties appears challenging, but vital to get better insight of the relationship between light and fruit attributes. In this study, nine solid phantoms capturing the ranges of absorption (μa) and reduced scattering (μs') coefficients in fruit were analysed non-destructively using laser-induced backscattering imaging (LLBI) at 1060 nm. Data analysis of LLBI was carried out on the diffuse reflectance, attenuation profile obtained by means of Farrell's diffusion theory either calculating μa [cm-1] and μs' [cm-1] in one fitting step or fitting only one optical variable and providing the other one from a destructive analysis. The nondestructive approach was approved when calculating one unknown coefficient non-destructively, while no ability of the method was found to analysis both, μa and μs', non-destructively. Setting μs' according to destructive photon density wave (PDW) spectroscopy and fitting μa resulted in root mean square error (rmse) of 18.7\% in comparison to fitting μs' resulting in rmse of 2.6\%, pointing to decreased measuring uncertainty, when the highly variable μa was known. The approach was tested on European pear, utilizing destructive PDW spectroscopy for setting one variable, while LLBI was applied for calculating the remaining coefficient. Results indicated that the optical properties of pear obtained from PDW spectroscopy as well as LLBI changed concurrently in correspondence to water content mainly. A destructive batch-wise analysis of μs' and online analysis of μa may be considered in future developments for improved fruit sorting results, when considering fruit with high variability of μs'.}, language = {en} } @article{ZuhrtNeumannZuelicke1999, author = {Zuhrt, Christian and Neumann, Rainer and Z{\"u}licke, Lutz}, title = {Investigation of vibrational states of the ArHCl+ cation in the electronic ground state}, year = {1999}, language = {en} } @article{ZuehlkeMeilingRoderetal.2021, author = {Z{\"u}hlke, Martin and Meiling, Till Thomas and Roder, Phillip and Riebe, Daniel and Beitz, Toralf and Bald, Ilko and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Janßen, Traute and Erhard, Marcel and Repp, Alexander}, title = {Photodynamic inactivation of E. coli bacteria via carbon nanodots}, series = {ACS omega / American Chemical Society}, volume = {6}, journal = {ACS omega / American Chemical Society}, number = {37}, publisher = {ACS Publications}, address = {Washington, DC}, issn = {2470-1343}, doi = {10.1021/acsomega.1c01700}, pages = {23742 -- 23749}, year = {2021}, abstract = {The increasing development of antibiotic resistance in bacteria has been a major problem for years, both in human and veterinary medicine. Prophylactic measures, such as the use of vaccines, are of great importance in reducing the use of antibiotics in livestock. These vaccines are mainly produced based on formaldehyde inactivation. However, the latter damages the recognition elements of the bacterial proteins and thus could reduce the immune response in the animal. An alternative inactivation method developed in this work is based on gentle photodynamic inactivation using carbon nanodots (CNDs) at excitation wavelengths λex > 290 nm. The photodynamic inactivation was characterized on the nonvirulent laboratory strain Escherichia coli K12 using synthesized CNDs. For a gentle inactivation, the CNDs must be absorbed into the cytoplasm of the E. coli cell. Thus, the inactivation through photoinduced formation of reactive oxygen species only takes place inside the bacterium, which means that the outer membrane is neither damaged nor altered. The loading of the CNDs into E. coli was examined using fluorescence microscopy. Complete loading of the bacterial cells could be achieved in less than 10 min. These studies revealed a reversible uptake process allowing the recovery and reuse of the CNDs after irradiation and before the administration of the vaccine. The success of photodynamic inactivation was verified by viability assays on agar. In a homemade flow photoreactor, the fastest successful irradiation of the bacteria could be carried out in 34 s. Therefore, the photodynamic inactivation based on CNDs is very effective. The membrane integrity of the bacteria after irradiation was verified by slide agglutination and atomic force microscopy. The method developed for the laboratory strain E. coli K12 could then be successfully applied to the important avian pathogens Bordetella avium and Ornithobacterium rhinotracheale to aid the development of novel vaccines.}, language = {en} } @article{ZuehlkeRiebeBeitzetal.2016, author = {Z{\"u}hlke, Martin and Riebe, Daniel and Beitz, Toralf and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Andreotti, Sandro and Reinert, Knut and Zenichowski, Karl and Diener, Marc}, title = {High-performance liquid chromatography with electrospray ionization ion mobility spectrometry: Characterization, data management, and applications}, series = {Journal of separation science}, volume = {39}, journal = {Journal of separation science}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1615-9306}, doi = {10.1002/jssc.201600749}, pages = {4756 -- 4764}, year = {2016}, abstract = {The combination of high-performance liquid chromatography and electrospray ionization ion mobility spectrometry facilitates the two-dimensional separation of complex mixtures in the retention and drift time plane. The ion mobility spectrometer presented here was optimized for flow rates customarily used in high-performance liquid chromatography between 100 and 1500 mu L/min. The characterization of the system with respect to such parameters as the peak capacity of each time dimension and of the 2D spectrum was carried out based on a separation of a pesticide mixture containing 24 substances. While the total ion current chromatogram is coarsely resolved, exhibiting coelutions for a number of compounds, all substances can be separately detected in the 2D plane due to the orthogonality of the separations in retention and drift dimensions. Another major advantage of the ion mobility detector is the identification of substances based on their characteristic mobilities. Electrospray ionization allows the detection of substances lacking a chromophore. As an example, the separation of a mixture of 18 amino acids is presented. A software built upon the free mass spectrometry package OpenMS was developed for processing the extensive 2D data. The different processing steps are implemented as separate modules which can be arranged in a graphic workflow facilitating automated processing of data.}, language = {en} } @article{ZuehlkeRiebeBeitzetal.2015, author = {Z{\"u}hlke, Martin and Riebe, Daniel and Beitz, Toralf and L{\"o}hmannsr{\"o}ben, Hans-Gerd and Zenichowski, Karl and Diener, Marc and Linscheid, Michael W.}, title = {An electrospray ionization-ion mobility spectrometer as detector for high-performance liquid chromatography}, series = {European journal of mass spectrometry}, volume = {21}, journal = {European journal of mass spectrometry}, number = {3}, publisher = {WeltTrends}, address = {Sussex}, issn = {1469-0667}, doi = {10.1255/ejms.1367}, pages = {391 -- 402}, year = {2015}, abstract = {The application of electrospray ionization (ESI) ion mobility (IM) spectrometry on the detection end of a high-performance liquid chromatograph has been a subject of study for some time. So far, this method has been limited to low flow rates or has required splitting of the liquid flow. This work presents a novel concept of an ESI source facilitating the stable operation of the spectrometer at flow rates between 10 mu L min(-1) and 1500 mu L min(-1) without flow splitting, advancing the T-cylinder design developed by Kurnin and co-workers. Flow rates eight times faster than previously reported were achieved because of a more efficient dispersion of the liquid at increased electrospray voltages combined with nebulization by a sheath gas. Imaging revealed the spray operation to be in a rotationally symmetric multijet-mode. The novel ESI-IM spectrometer tolerates high water contents (<= 90\%) and electrolyte concentrations up to 10 mM, meeting another condition required of high-performance liquid chromatography (HPLC) detectors. Limits of detection of 50 nM for promazine in the positive mode and 1 mu M for 1,3-dinitrobenzene in the negative mode were established. Three mixtures of reduced complexity (five surfactants, four neuroleptics, and two isomers) were separated in the millisecond regime in stand-alone operation of the spectrometer. Separations of two more complex mixtures (five neuroleptics and 13 pesticides) demonstrate the application of the spectrometer as an HPLC detector. The examples illustrate the advantages of the spectrometer over the established diode array detector, in terms of additional IM separation of substances not fully separated in the retention time domain as well as identification of substances based on their characteristic IMs.}, language = {en} } @article{ZuehlkeSassRiebeetal.2017, author = {Z{\"u}hlke, Martin and Sass, Stephan and Riebe, Daniel and Beitz, Toralf and L{\"o}hmannsr{\"o}ben, Hans-Gerd}, title = {Real-Time Reaction Monitoring of an Organic Multistep Reaction by Electrospray Ionization-Ion Mobility Spectrometry}, series = {ChemPlusChem}, volume = {82}, journal = {ChemPlusChem}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {2192-6506}, doi = {10.1002/cplu.201700296}, pages = {1266 -- 1273}, year = {2017}, abstract = {The capability of electrospray ionization (ESI)-ion mobility (IM) spectrometry for reaction monitoring is assessed both as a stand-alone real-time technique and in combination with HPLC. A three-step chemical reaction, consisting of a Williamson ether synthesis followed by a hydrogenation and an N-alkylation step, is chosen for demonstration. Intermediates and products are determined with a drift time to mass-per-charge correlation. Addition of an HPLC column to the setup increases the separation power and allows the determination of further species. Monitoring of the intensities of the various species over the reaction time allows the detection of the end of reaction, determination of the rate-limiting step, observation of the system response in discontinuous processes, and optimization of the mass ratios of the starting materials. However, charge competition in ESI influences the quantitative detection of substances in the reaction mixture. Therefore, two different methods are investigated, which allow the quantification and investigation of reaction kinetics. The first method is based on the pre-separation of the compounds on an HPLC column and their subsequent individual detection in the ESI-IM spectrometer. The second method involves an extended calibration procedure, which considers charge competition effects and facilitates nearly real-time quantification.}, language = {en} } @article{ZuehlkeZenichowskiRiebeetal.2017, author = {Z{\"u}hlke, Martin and Zenichowski, Karl and Riebe, Daniel and Beitz, Toralf and L{\"o}hmannsr{\"o}ben, Hans-Gerd}, title = {Subambient pressure electrospray ionization ion mobility spectrometry}, series = {International journal for ion mobility spectrometry : official publication of the International Society for Ion Mobility Spectrometry}, volume = {20}, journal = {International journal for ion mobility spectrometry : official publication of the International Society for Ion Mobility Spectrometry}, publisher = {Springer}, address = {Heidelberg}, issn = {1435-6163}, doi = {10.1007/s12127-017-0215-x}, pages = {47 -- 56}, year = {2017}, abstract = {The pressure dependence of sheath gas assisted electrospray ionization (ESI) was investigated based on two complementary experimental setups, namely an ESI-ion mobility (IM) spectrometer and an ESI capillary - Faraday plate setup housed in an optically accessible vacuum chamber. The ESI-IM spectrometer is capable of working in the pressure range between 300 and 1000 mbar. Another aim was the assessment of the analytical capabilities of a subambient pressure ESI-IM spectrometer. The pressure dependence of ESI was characterized by imaging the electrospray and recording current-voltage (I-U) curves. Qualitatively different behavior was observed in both setups. While the current rises continuously with the voltage in the capillary-plate setup, a sharp increase of the current was measured in the IM spectrometer above a pressure-dependent threshold voltage. The different character can be attributed to the detection of different species in both experiments. In the capillary-plate experiment, a multitude of charged species are detected while only desolvated ions attribute to the IM spectrometer signal. This finding demonstrates the utility of IM spectrometry for the characterization of ESI, since in contrast to the capillary-plate setup, the release of ions from the electrospray droplets can be observed. The I-U curves change significantly with pressure. An important result is the reduction of the maximum current with decreasing pressure. The connected loss of ionization efficiency can be compensated by a more efficient transfer of ions in the IM spectrometer at increased E/N. Thus, similar limits of detection could be obtained at 500 mbar and 1 bar.}, language = {en} } @article{ZuelickeRagnettiNeumann1997, author = {Z{\"u}licke, Lutz and Ragnetti, Francesca and Neumann, Rainer}, title = {Ionized Van-der-Waals systems : structure and interactions}, year = {1997}, language = {en} } @article{ZuelickeRagnettiNeumannetal.1996, author = {Z{\"u}licke, Lutz and Ragnetti, Francesca and Neumann, Rainer and Zuhrt, Christian}, title = {Ionized Van-der-Waals systems : structure and interactions}, series = {Technical Report / Institute of Physical and Theoretical Chemistry, Potsdam}, volume = {1996, 01}, journal = {Technical Report / Institute of Physical and Theoretical Chemistry, Potsdam}, publisher = {Univ.}, address = {Potsdam}, pages = {46 S.}, year = {1996}, language = {en} } @article{ZuelickeZuhrtChapuisatetal.1994, author = {Z{\"u}licke, Lutz and Zuhrt, Christian and Chapuisat, Xavier and Saint-Esp{\´e}s, C{\´e}cile}, title = {Internal dynamics of simple floppy molecules}, year = {1994}, language = {en} } @article{OenerQuerebilloDavidetal.2018, author = {{\"O}ner, Ibrahim Halil and Querebillo, Christine Joy and David, Christin and Gernert, Ulrich and Walter, Carsten and Driess, Matthias and Leimk{\"u}hler, Silke and Ly, Khoa Hoang and Weidinger, Inez M.}, title = {High electromagnetic field enhancement of TiO2 nanotube electrodes}, series = {Angewandte Chemie : a journal of the Gesellschaft Deutscher Chemiker ; International edition}, volume = {57}, journal = {Angewandte Chemie : a journal of the Gesellschaft Deutscher Chemiker ; International edition}, number = {24}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1433-7851}, doi = {10.1002/anie.201802597}, pages = {7225 -- 7229}, year = {2018}, abstract = {We present the fabrication of TiO2 nanotube electrodes with high biocompatibility and extraordinary spectroscopic properties. Intense surface-enhanced resonance Raman signals of the heme unit of the redox enzyme Cytochromeb(5) were observed upon covalent immobilization of the protein matrix on the TiO2 surface, revealing overall preserved structural integrity and redox behavior. The enhancement factor could be rationally controlled by varying the electrode annealing temperature, reaching a record maximum value of over 70 at 475 degrees C. For the first time, such high values are reported for non-directly surface-interacting probes, for which the involvement of charge-transfer processes in signal amplification can be excluded. The origin of the surface enhancement is exclusively attributed to enhanced localized electric fields resulting from the specific optical properties of the nanotubular geometry of the electrode.}, language = {en} } @article{OPUS4-15433, title = {Preparation of simple and mixed nickel and cobalt molybdates using hybrid precursors made from an ordered polymer matrix and inorganic salts}, year = {2004}, abstract = {The amphiphilic poly(ampholyte) poly(N,N-diallyl-N-hexylamine-alt-maleic acid), bearing simultaneously carboxylic acids, amines and hydrocarbon side chains, was used as a matrix to stabilize inorganic ion species (anionic as well as cationic) generated in aqueous solution from Ni(NO3)(2).6H(2)O, Co(NO3)(2).6H(2)O and (NH4)2MoO(4). Drying produces hybrid organic-inorganic blends which, due to the amphiphilicity of the copolymer, exhibit supramolecular organization in the bulk. Solid state studies show that up to two moles of metal cations (alone or together with metal anions) per repeat unit of the copolymer can be blended without loss of homogeneity in the hybrid material. A systematic screening permitted the determination of the optimal conditions for the preparation of homogeneous blends. Thermal treatment of the hybrid materials produces simple and mixed nickel and/or cobalt molybdates. The alpha- as well as the P- phase were obtained, and the mixed structures are solid solutions of simple NiMoO4 and CoMoO4}, language = {en} } @book{OPUS4-4353, title = {EUCHIS '99 : proceedings of the 3rd international conference of the European Chitin Society, Potsdam, Germany, Aug. 31 - Sept. 3, 1999}, isbn = {978-3-980649-45-2}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-45492}, publisher = {Universit{\"a}t Potsdam}, year = {2000}, abstract = {Contents: Production and Applications of Chitin and Chitosan Krill as a promising raw material for the production of chitin in Europe - Containerized plant for producing chitin - Preparation and characterization of chitosan from Mucorales - Chitosan from Absidia orchidis - Scaling up of lactic acid fermentation of prawn wastes in packed-bed column reactor for chitin recovery - Preparation of chitin by acetic acid fermentation - Inter-source reproducibility of the chitin deacetylation process - Comparative analysis of chitosans from insects and crustacea - Effect of the rate of deacetylation on the physico-chemical properties of cuttlefish chitosan - Deacetylation of chitin by fungal enzymes - Production of partially degraded chitosan with desired molecular weight - Chitin-containing materials Mycoton for wounds treatment - Biological activity of selected forms of chitosan - Application of chitosan on the preservation quality of cut flowers - Preparation and characterization of chitosan films: application in cell cultures - Transport phenomena in chitin gels - Symplex membranes of chitosan and sulphoethylcellulose - Preparation and use of chitosan-Ca pectinate pellets - Bioseparation of protein from cheese whey by using chitosan coagulation and ultrafiltration membranes - Preparation of silk fibroin/chitosan fiber - Preparation of paper sheets containing microcrystalline chitosan - Applications of chitosan in textile printing - Permanent modification of fibrous materials with biopolymers - Ion exchanger from chitosan - Chitosan in waste water treatment - The immobilization of tyrosinase on chitin and chitosan and its possible use in wastewater treatment - Utilization of modified chitosan in aqueous system treatment Biomaterials Chemical and preclinical studies on 6-oxychitin - Diverse biological effects of fungal chitin-glucan complex - Effect of concentration of neutralizing agent on chitosan membrane properties - Preliminary investigation of the compatibility of a chitosan-based peritoneal dialysis solution - Influence of chitosan on the growth of several cellular lines - A new chitosan containing phosphonic group with chelating properties - Biocompatibility of chitin materials using cell culture method Oral Administration of Chitosan Recent results in the oral administration of chitosan - Reduction of absorption of dietary lipids and cholesterol by chitosan, its derivatives and special formulations - Chitosan in weight reduction: results from a large scale consumer study - Conformation of chitosan ascorbic acid salt - Trimethylated chitosans as safe absorption enhancers for transmucosal delivery of peptide drugs - Chitosan derivates as intestinal penetration enhancers of the peptide drug buserelin in vivo and in vitro - Chitosan microparticles for oral vaccination: optimization and characterization - Effect of chitosan in enhancing drug delivery across buccal mucosa - Influence of chitosans on permeability of human intestinal epithelial (Caco-2) cells: The effect of molecular weight, degree of deacetylation and exposure time - Oral polymeric N-acetyl-D-glucosamine as potential treatment for patients with osteoarthritis - Clinicoimmunological efficiency of the chitin-containing drug Mycoton in complex treatment of a chronic hepatitis - Interactions of chitin, chitosan, N-laurylchitosan, and N-dimethylaminopropyl chitosan with olive oil - The chitin-containing preparation Mycoton in a pediatric gastroenterology case - Antifungal activity and release behaviour of cross-linked chitosan films incorporated with chlorhexidine gluconate - Release of N-acetyl-D-glucosamine from chitosan in saliva - Physical and Physicochemical Properties Recent approach of metal binding by chitosan and derivatives - As(V) sorption on molybdate-impregnated chitosan gel beads (MICB) - Influence of medium pH on the biosorption of heavy metals by chitin-containing sorbent Mycoton - Comparative studies on molecular chain parameters of polyelectrolyte chains: the stiffness parameter B and temperature coefficient of intrinsic viscosity of chitosans and poly(diallyldimethylammonium chloride) - Crystalline behavior of chitosan - The relationship between the crystallinity and degree of deacetylation of chitin from crab shell - Reversible water-swellable chitin gel: modulation of swellability - Syneresis aspects of chitosan based gel systems - In situ chitosan gelation using the enzyme tyrosinase - Preparation and characterization of controlling pore size chitosan membranes - Fabrication of porous chitin matrices - Changes of polydispersity and limited molecular weight of ultrasonic treated chitosan - A statistical evaluation of IR spectroscopic methods to determine the degree of acetylation of ?-chitin and chitosan - Products of alkaline hydrolysis of dibutyrylchitin: chemical composition and DSC investigation - Chitosan emulsification properties Chemistry of Chitin and Chitosan Chemically modified chitinous materials: preparation and properties - Progress on the modification of chitosan - The graft copolymerization of chitosan with methyl acrylate using an organohalide-manganese carbonyl coinitiator system - Grafting of 4-vinylpyridine, maleic acid and maleic anhydride onto chitin and chitosan - Peptide synthesis on chitosan/chitin - Graft copolymerization of methyl methacrylate onto mercapto-chitin - Thermal depolymerization of chitosan salts - Radiolysis and sonolysis of chitosan - two convenient techniques for a controlled reduction of molecular weight - Thermal and UV degradation of chitosan - Heat-induced physicochemical changes in highly deacetylated chitosan - Chitosan fiber and its chemical N-modification at the fiber state for use as functional materials - Preparation of a fiber reactive chitosan derivative with enhanced microbial activity - Chromatographic separation of rare earths with complexane types of chemically modified chitosan - The effects of detergents on chitosan - Chitosan-alginate PEC films prepared from chitosan of different molecular weights - Enzymology of Chitin and Chitosan Biosynthesis and Degradation Enzymes of chitin metabolism for the design of antifungals - Enzymatic degradation of chitin by microorganisms - Kinetic behaviours of chitinase isozymes - An acidic chitinase from gizzards of broiler (Gallus gallus L.) - On the contribution of conserved acidic residues to catalytic activity of chitinase B from Serratia marcescens - Detection, isolation and preliminary characterisation of a new hyperthermophilic chitinase from the anaerobic archaebacterium Thermococcus chitonophagus - Biochemical and genetic engineering studies on chitinase A from Serratia marcescens - Induction of chitinase production by Serratia marcescens, using a synthetic N-acetylglucosamine derivative - Libraries of chito-oligosaccharides of mixed acetylation patterns and their interactions with chitinases - Approaches towards the design of new chitinase inhibitors - Allosamidin inhibits the fragmentation and autolysis of Penicillium chrysogenum - cDNA encoding chitinase in the midge, Chironomus tentans - Extraction and purification of chitosanase from Bacillus cereus - Substrate binding mechanism of chitosanase from Streptomyces sp. N174 - Chitosanase-catalyzed hydrolysis of 4-methylumbelliferyl ?-chitotrioside - A rust fungus turns chitin into chitosan upon plant tissue colonization to evade recognition by the host - Antibiotic kanosamine is an inhibitor of chitin biosynthesis in fungi - PCR amplification of chitin deacetylase genes - Amplification of antifungal effect of GlcN-6-P synthase and chitin synthase inhibitors - ?-N-Acetylhexosaminidases: two enzyme families, two mechanisms - Purification and characterisation of chitin deacetylase from Absidia orchidis - Effect of aluminium ion on hydrolysis reaction of carboxymethyl- and dihydroxypropyl-chitin with lysozyme - Structure and function relatioship of human N-acetyl-D-glucosamine 2-epimerase (renin binding protein) - Identification of active site residue(s)}, language = {en} } @book{OPUS4-27424, title = {Journal of the science of food and agriculture}, editor = {Schwenke, Klaus Dieter}, publisher = {Wiley-VCH}, address = {Chichester}, year = {1995}, language = {en} } @book{OPUS4-29390, title = {Chemical Physics}, editor = {Z{\"u}licke, Lutz}, publisher = {Elsevier}, address = {Amsterdam [u.a.]}, year = {1991}, language = {en} } @book{OPUS4-30767, title = {Advances in chitin science}, editor = {Struszczyk, Henryk and Peter, Martin G. and Domard, Alain and Pospieszny, Henryk}, year = {1996}, language = {en} } @article{OPUS4-10587, title = {DFT-GIAO-NBO and 13C NMR study of the delta-syn-axial effect in 2,4-disubstituted adamantanes}, issn = {0749-1581}, doi = {10.1002/Mrc.2333}, year = {2008}, abstract = {Six groups of diastereomeric 2,4-disubstituted adamantanes were studied with DFT-GIAO-NBO (natural orbital analysis) methods. The calculated 13C chemical shifts reproduce well the experimental data. It was found that among all diastereomers, those bearing substituents in -syn-axial positions showed the largest overall deshielding, i.e. the sum of all 13C chemical shifts [;;(13C)] was the greatest and also had the highest delocalization contribution to the molecular energy evaluated with NBO. The higher delocalization energy is proposed to be the origin of the deshielding -syn-axial effect}, language = {en} } @article{OPUS4-10769, title = {Synthesis and conformational analysis of phenyl-substituted 1,3,2-oxazaphosphino[4,3-a]- and 1,2,3- oxathiazino[4,3-a]isoquinolines}, year = {2008}, abstract = {Through the ring closures of tetrahydroisoquinoline 1,3-amino alcohols bearing a phenyl group in the side- chain, diastereomers of novel 1- or 2-phenyl-substituted 1,3,2-oxazaphosphino[4,3-a]isoquinoline 4-oxides, and 1,2,3- oxathiazino[4,3-a]isoquinoline 4-oxides and 4,4-dioxides were prepared. NMR analysis and DFT calculations on the prepared tetrahydroisoquinoline-condensed 1,2,3-heterocycles revealed that their conformational equilibria of cis1-trans-cis2 type are influenced by the relative configuration of P-4 in the 1,3,2-oxazaphosphinanes, and by the position of the phenyl group in the 1,2,3-oxathiazines.}, language = {en} }