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BISSINGER, V.; TITTEL, J.: Process rates and growth limiting factors of planktonic algae (Chlamydomonas sp.) from extremely acidic (pH 2,5 - 3) mining lakes in Germany ; BORK, H.-R. et al.: Erodierte Autos und Brunnen in Oregon, USA ; BRONSTERT, A. et al.: Bewirtschaftunsmöglichkeiten im Einzugsgebiet der Havel ; JELTSCH, F. et al.: Beweidung als Degradationsfaktor in ariden und semiariden Weidesystemen ; JELTSCH, F. et al.: Entstehung und Bedeutung räumlicher Vegetationsstrukturen in Trockensavannen: Baum-Graskoexistenz und Artenvielfalt ; JESSEL, B. et al.: Bodenbewertung für Planungs- und Zulassungsverfahren in Brandenburg ; JESSEL, B.; ZSCHALICH, A.: Erarbeitung von Ausgleichs- und Ersatzmaßnahmen für die Wert- und Funktionselemente des Landschaftsbildes ; RÖßLING, H. et al.: Umsetzung von Ausgleichs- und Ersatzmaßnahmen beim Ausbau der Bundesautobahn A 9 ; SPINDLER, J.; GAEDKE, U.: Estimating production in plankton food webs from biomass size spectra and allometric relationships ; TIELBÖRGER, K. et al.: Sukzessionsprozesse in einem Sanddünengebiet nach Ausschluß von Beweidung ; TIELBÖRGER, K. et al.: Populationsdynamische Funktionen von Ausbreitung und Dormanz ; TIELBÖRGER, K. et al.: Raum-zeitliche Populationsdynamik von einjährigen Wüstenpflanzen ; TITTEL, J. et al.: Ressourcennutzung und -weitergabe im planktischen Nahrungsnetz eines extrem sauren (pH 2,7) Tagebausees ; WALLSCHLÄGER, D.; WIEGLEB, G.: Offenland-Management auf ehemaligen und in Nutzung befindlichen Truppenübungsplätzen im pleistozänen Flachland Nordostdeutschlands: Naturschutzfachliche Grundlagen und praktische Anwendungen ; WEITHOFF, G.; GAEDKE, U.: Planktische Räuber-Beute-Systeme: Experimentelle Untersuchung von ökologischen Synchronisationen
Zusammenfassung Eine Diskussion um das künftige Verhältnis von Landschaftsplanung und Strategischer Umweltprüfung (SUP) hat von den unterschiedlichen Aufgabenstellungen beider Instrumente auszugehen (Umweltfolgenprüfung durch die SUP und konzeptionell-planungsbezogener Ansatz der Landschaftsplanung). Um Überschneidungsbereiche von SUP und Landschaftsplanung zu identifizieren, werden in dem Beitrag verfahrensmäßige und inhaltliche Aspekte getrennt betrachtet. Deutlich wird, dass die Landschaftsplanung für den Bereich Natur und Landschaft eine zentrale Daten- und Informationsgrundlage für die SUP sein kann. Es bleibt zu hoffen, dass vor diesem Hintergrund die im Entwurf zu einem SUP-Stammgesetz vom Juli 2003 vorgesehene SUP- Pflicht für Landschaftsplanungen noch einmal überdacht wird. Bei der Zuarbeit zur SUP besteht für die Landschaftsplanung sowohl die Gefahr einer Überfrachtung als auch die Chance für eine substanzielle inhaltliche Weiterentwicklung: Insbesondere können von der SUP Impulse für mehr Prozesshaftigkeit der Landschaftsplanungen, eine größere Aktualität sowie häufigere und zielgenauere Fortschreibungen ihrer Planwerke ausgehen. Eine zu starke Fixierung der Landschaftsplanung auf die SUP würde allerdings zu einer zu starken fachlichen Einengung auf die Folgenprüfung führen. Um dem zu begegnen, scheint eine flexible Kombination beider Instrumente zielführend. Diese kann erreicht werden, indem die Landschaftsplanung einzelne problembezogen angelegte Module zur SUP erarbeitet und damit für sie den wesentlichen Baustein für die Aufarbeitung der Naturschutzaspekte liefert. A discussion abuot the future relation of Landscape Planning and Strategic Environmental Assessment (SEA) has to base on the different tasks of both instruments (analysis of environmental consequences by the SEA and conceptional approach related to planning by Landscape Planning). In order to identify overlapping parts of SEA and Landscape Planning the study separately investigates aspects of procedure and content. The results show that landscape planning can provide a central base of data and information for the SEA. Against this setting the draft of a SEA core law of July 2003 requiring the conduction of SEA for Landscape Planning will hopefully be reconsidered. The contribution of SEA to Landscape Planning on the one hand holds the risk of overloading but also offers the chance for a substantial further development: The SEA can improve the process aspect of Landscape Planning as well as stimulate more topicality and more frequent and exact updating of planning projects. On the other hand, however, a very strong specification of Landscape Planning towards SEA would lead to a restriction on the analysis of environmental consequences. A flexible combination of both instruments appears to fulfil the target. This means that Landscape Planning develops individual problem-related modules of SEA providing the fundamental component to deal with the nature conservation aspects.
The new tetrathiacrown ethers maleonitrile-tetrathia-12-crown-4 (mn12S(4)) and maleonitrile-tetrathia-13-crown- 4 (mn13S(4)) have been prepared and characterised by X-ray crystallographic analysis. These crown ethers form 2:1, 3:2 and 1: 1 complexes with AgY (Y = BF4, PF6). The crystal structures of [Ag(mn12S(4))(2)]BF4 (3a), [Ag(mn13S(4))(2)]BF4 (4a) and [Ag-2(mn13S(4))(3)](PF6)(2) (6b) have been determined. Compound 3a contains the centrosymmetric sandwich complex cation [Ag(mn12S(4))(2)](+) where each mn12S(4) ligand is coordinated to the Ag centre in an endo manner through all four S atoms. The 2:1 complex [Ag(mn12S(4))(2)](+) is the first sandwich complex with a tetrathiacrown ether and the first complex with an octa(thioether) coordination sphere. The crystal structure of compound 4a also reveals a 2:1 complex. This complex, [Ag(mnl3S(4))(2)](+), exhibits a half-sandwich structure. One mn13S(4) ligand coordinates to Ag+ by all four S donor atoms and the other 13S(4) crown by only one S atom. Compound 6b contains a dinuclear Ag complex. The Ag complexes 3a,b-8a,b were also studied by electrospray ionisation mass spectrometry. Collision-induced dissociation (CID) was used to compare the relative stability of 2:1 complexes [AgL2]+ and 1:1 complexes [AgL](+) (L = mn12S(4), mn13S(4)). The C-13 NMR chemical shifts of 2:1 and 1:1 Ag complexes and their corresponding free ligands were also estimated and compared. The free energy of the barrier of ring inversion (Delta G(double dagger)) for [Ag(mn12S(4))(2)](+) was determined to be 64 kJmol(-1).
The complexes [(HgCl2)(2)((ch)(2)30S(4)O(6))] (1), [HgCl,(mn21S(2)O(5))] (2), [HgCl2(ch18S(2)O(4))] (3) and [HgI(meb12S(2)O(2))](2)[Hg2I6] (4) have been synthesized, characterized and their crystal structures were determined. In [(HgCl2)(2)((ch)(2)3OS(4)O(6))] two HgCl2 units are discretely bonded within the ligand cavity of the 30-membered dichinoxaline-tetrathia-30-crown-10 ((ch)(2)30S(4)O(6)) forming a binuclear complex. HgCl2 forms I : I "in-cavity" complexes with the 21-membered maleonitrile-dithia-21-crown-7(mn21S(2)O(5)) ligand and the 18-membered chinoxaline- dithia-18-crown-6 (ch18S(2)O(4)) ligand, respectively. The 12-membered 4-methyl-benzo-dithia-12-crown-4 (meb12S(2)O(2)) ligand gave with two equivalents HgI2 the compound [HgI(meb12S(2)O(2))](2)[Hg2I6]. In the cation [HgI(meb12S(2)O(2))](+) meb12S(2)O(2) forms with the cation HgI+ a half-sandwich complex
Electrospray ionization was employed to study the mass spectrometric behavior of the maleonitrile tetrathiacrown ethers mn12S(4) (1) and mn13S(4) (2) and maleonitrile pentathiacrown ether mn15S(5) (3) and of their complexes with various metal salts (MX2, M=Pd, Pt, Ni, Co, Fe; X=Cl, CrCl3, Ni(BF4)(2), TIPF6 or Cd(NO3)(2)) and Cu(SO3CF3)(2). Both singly charged, [MXL](+) and [MXL2]+, and doubly charged complexes, [MLn](2+) (n = 2-5), were observed. The formation of the different complexes consisting of the transition metal ion, the counterion and the various crown ethers and their subsequent dissociation was also studied by collision-induced dissociation measurements which were also used to evaluate the relative stabilities of the complexes. It was found that the collisional voltages for the dissociation of the complexes were generally greater in the [MXL](+) complexes than in the corresponding [MXL2]+ complexes. Copyright (c) 2006 John Wiley & Sons, Ltd
Homoleptic Ni-II and Fe-II complexes of the "large-surface" phenanthroline-type ligand 1,12-diazaperylene (dap), [Ni(dap)(3)](BF4)(2) (1) and [Fe(dap)(3)](PF6)(2) (2), respectively, were synthesized. In the crystal structure the complex cation [M(dap)(3)](2+) (M = Ni, Fe) exhibits C-3 symmetry and interacts with three other cations by pi-pi stacking. It forms a new metalla-supramolecular assembly with a honeycomb structure containing nanochannels running parallel to the crystallographic c axis. Aggregation by pi-pi stacking between metal complexes of "large-surface" ligands should give new perspectives for inorganic supramolecular chemistry.
The synthesis and single crystal X-ray structures of eight AgI, HgII, and PtII complexes with the thiacrown ethers maleonitrile-tetrathia-12-crown-4 (mn12S4), maleonitrile-tetrathia-13-crown-4 (mn13S4), and maleonitrile- pentathia-15-crown-5 (mn15S5) (1) are reported. The ligand mn15S5 was synthesized for the first time and characterized by X-ray diffraction. With silver(I) perchlorate and silver(I) tetrafluoroborate it forms the chiral complexes [Ag(mn15S5)]ClO4·CH3NO2 (2) and [Ag(mn15S5)]BF4·CH3NO2·0.25H2O (3) with half-sandwich moieties. AgI is located in a distorted tetrahedral coordination environment, involving three sulfur atoms of the crown cycle and a fourth one of the adjacent half-sandwich moiety, forming a helical structure. The reaction of Hg(ClO4)2 with mn13S4 yielded the dinuclear complex [Hg2(mn13S4)3](ClO4)4 (4) containing two half-sandwich moieties with a third ligand molecule as a bridging unit. Mercury(II) chloride and mercury(II) iodide react with mn12S4 and mn13S4 to form complexes of the general composition [HgX2(L)] (X = Cl, I; L = mn12S4, mn13S4): [HgCl2(mn12S4)] (5), [HgI2(mn12S4)] (6), [HgCl2(mn13S4)] (7) or [HgX2(L)2] (X = I; L = mn13S4): [HgI2(mn13S4)2] (8). Only one or two sulfur atoms of the ligand are involved in the complexation, and chain or ribbon structures are formed. In these compounds the HgX2 units (X = Cl, I) are preserved, coordinated by sulfur atoms of bridging mn12S4 or mn13S4 ligands. In all complexes of this type, the metal atoms are not coordinated inside the cavity, but in an exocyclic mode, because the diameter of the macrocycle is too small. Additionally, the PtCl2 complex of mn12S4 was investigated, where PtII is coordinated in an exocyclic mode forming the complex [PtCl2(mn12S4)] (9). Two of the four sulfur atoms of the macrocycle are bonded to the metal giving together with both chlorine atoms a square-planar coordination geometry. Together with a long-range interaction with a further sulfur atom of the macrocycle a square-pyramidal coordination environment is formed.
Narrow channels with polar walls are the structural and functional features responsible for the high capacity of a zinc-organic framework based on an imidazolate-amide-imidate ligand for the uptake of H2 and CO2 (see structure: orange Zn, blue N, red O, dark gray C, light gray H). The rigid and stable chelating ligand was synthesized in situ by partial hydrolysis of a dicyanoimidazole compound.