Go toArchive
Browse byFacets
Bookbag ( 0 )
Facet   section ZfN Section B:Volume 047  [X]
Results  290 Items
Sorted by   
Publication Year
1992 (290)
101Author    Henri Brunner, Paul BrandlRequires cookie*
 Title    Asymmetrische Katalysen, 76 [1]  
 Abstract    Rh-katalysierte enantioselektive Hydrosilylierung von Acetophenon mit einem polymergebundenen Pyridinoxazolin Asymmetric Catalysis, 76 [1] Rh-Catalyzed Enantioseleetive Hydrosilylation o f Aeetophenone by a Polymer-Bound Pyridineoxazoline A n organ isch e C hem ie der U n iversität R egensburg, U niversitätsstraße 31, D -W -8400 R egensburg Herrn Prof. Dr. W. Beck zum 60. Geburtstag gew idm et Z. N aturforsch. 47b, 6 0 9 -6 1 3 (1992); ein gegan gen am 18. Juli 1991 O ptically A ctive L igands, P olystyrene-B oun d P yrid in eoxazolin e, E nan tioseleetive H ydrosilylation In the en an tioseleetive h yd rosilylation o f a e eto p h e n o n e with dip henylsilan e, a polystyrene-bound heterogeneous R h /p yrid in eoxazolin e catalyst achieved higher optical ind uction s than a com parable h o m o g en eo u s catalyst. A fter using the polym eric catalyst 8 —10 tim es, the catalyt­ ic activity decreased m arkedly and an inversion o f the product con figu ration w as observed, the enantiom eric excess rising to 92% ee. These results indicate that the polym eric catalyst c o n ­ tains several catalytically active species with different en antioselectivity and stability. 
  Reference    Z. Naturforsch. 47b, 609 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0609.pdf 
 Identifier    ZNB-1992-47b-0609 
 Volume    47 
102Author    H. P. Fritz, R. BertelmannRequires cookie*
 Title    Kationenleiter auf der Basis von Poly(maleinsäure) Cation Conductors Based on Polymaleic Acid  
 Abstract    A us dem A n organ isch -ch em isch en In stitut der T ech nischen U n iversität M ünchen, L ichtenbergstraße 4, D -W -8 0 4 6 G arching Herrn Prof. Dr. W. B eck zum 60. G eburtstag gew idm et 
  Reference    Z. Naturforsch. 47b, 614 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0614.pdf 
 Identifier    ZNB-1992-47b-0614 
 Volume    47 
103Author    Brigitte Lauerer3, A. Puschb, K. H. Stadler^, H. P. BoehmRequires cookie*
 Title    Adsorption of Tetrammine-carbonato and -cis-diaqua and Triethylenetetramine-carbonato and -as-diaqua Complexes of Cobalt(III) on Titanium Dioxide as Models for the Binding of Uranyl Ions from the Tricarbonatouranyl Complex Ion  
  Reference    Z. Naturforsch. 47b, 625 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0625.pdf 
 Identifier    ZNB-1992-47b-0625 
 Volume    47 
104Author    AzaborolylRequires cookie*
 Title    Azaborolyl-Komplexe, 27 Der 1 -ter f-Buty 1-2-methy l-3-(4-penten-1 -yl)-1H -1,2-azaboroly 1-Ring als bifunktioneller Ligand in Rhodiumkomplexen  
  Reference    Z. Naturforsch. 47b, 635 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0635.pdf 
 Identifier    ZNB-1992-47b-0635 
 Volume    47 
105Author    Hubert Schmidbaur, Albert Stützer, Peter BissingerRequires cookie*
 Title    Synthesis and Structure of Tetrakis(diphenyIphosphanyImethyI)methane and its Tetranuclear AuCl Complex  
 Abstract    A n organ isch -ch em isch es Institut der T echnischen U niversität M ünchen, L ichtenbergstraße 4, D -W -8046 G arching D edicated to Prof. W. Beck on the occasion o f his 60 th birthday 
  Reference    Z. Naturforsch. 47b, 640 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0640.pdf 
 Identifier    ZNB-1992-47b-0640 
 Volume    47 
106Author    Requires cookie*
 Title    Übergangsmetallkomplexe mit Schwefelliganden, LXXXV  
 Abstract    |Ni('buS4-C 2)]3, ein neuer Typ dreikerniger Ni-Komplexe (buS4 -C2' = 1,2-Bis(3,5-ditertiärbutyl-2-mercaptophenylthio)ethan(2 -)) Transition-M etal Complexes with Sulfur Ligands, LXXXV*. 
  Reference    Z. Naturforsch. 47b, 645 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0645.pdf 
 Identifier    ZNB-1992-47b-0645 
 Volume    47 
107Author    Requires cookie*
 Title    Selektive Ligandensubstitutionsreaktionen an Carbin-Wolframkomplexen des Typs IW(CPh)Br(CO)2L2] (L = Stickstoff-Donorligand)  
  Reference    Z. Naturforsch. 47b, 656 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0656.pdf 
 Identifier    ZNB-1992-47b-0656 
 Volume    47 
108Author    Bernd Wrackmeyer, Jürgen SchillerRequires cookie*
 Title    5N Nucelar Magnetic Resonance Study of Two-Coordinate Phosphorus Cations -Sign-Determination of Coupling Constants -Application of Two-Dimensional (2 D) Heteronuclear Shift Correlations  
  Reference    Z. Naturforsch. 47b, 662 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0662.pdf 
 Identifier    ZNB-1992-47b-0662 
 Volume    47 
109Author    O. H. Eyke, G. B. Euter, I.-P LorenzRequires cookie*
 Title    Darstellung  
 Abstract    , Reaktivität und Kristallstruktur von |(CO)3Mn(dppm)2(//-S)Rh(CO)I Synthesis, R eactivity an d C rystal S tru cture o f [(CO)3M n(dppm)2(//-S)Rh(CO)] The reaction o f [(CO)3Mn(dppm)-,Rh(CO)] (1) with H2S in dichloromethane yields [(CO)3M n(dppm)2(//-S)Rh(CO)] (2), which is characterized by IR, 31P {'H }, 'H, 13C {'H } nmr and mass spectra. The crystal structure o f 2 was determined by X-ray diffraction: space group P2j/m, Z = 4, a = 1232.6(3), b = 2558.8(4), c = 1640.8(2) pm, ß = 97.74(2)°, R /R w = 0.048/ 0.057. The dimeric com plex shows A-frame structure possessing a bridging sulfur and a sem i­ bridging CO group. 2 cannot be oxidized to the corresponding S 0 2 bridged complex [(C 0)3M n(dppm)2(/i-S 0 2)R h (C 0)] (3). The reaction o f 2 with SO-,, however, yields the S 0 2 bridged complex [(CO)2M n(dppm)2(/y-S)(//-SO^)Rh(CO)] (5); in dichloromethane 2 is readily chlorinated to afford the salt [(CO),M n(dppm)1(//-S)RhCl]Cl (4). 
  Reference    Z. Naturforsch. 47b, 668—6 (1992); eingegangen am 22. November 1991 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0668.pdf 
 Identifier    ZNB-1992-47b-0668 
 Volume    47 
110Author    Z. NaturforschRequires cookie*
 Title    B enzo-l,3,2-diselenazolylium Salts -Synthesis and Reactivity  
 Abstract    G o tth e lf W o lm ersh äu ser1*, W olfgang K aim b, G ert H eckm anna und A lexander L ich tb lau b Benzo-l,3,2-diselenazolylium chloride can be prepared analogously to the corresponding sulfur com pound. The cation has been characterized as its perchlorate by X-ray structure anal­ ysis. Reduction via the unstable neutral radical state finally affords the nitrogen-free 'dibenzo-tetraselenocine'. 
  Reference    Z. Naturforsch. 47b, 675—6 (1992); eingegangen am 16. Oktober 1991 
  Published    1992 
  Keywords    Heterocyclic C om pounds, Diselenazolylium Cations, Diselenazolyl Radicals, Selenium-Nitrogen C om pounds 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0675.pdf 
 Identifier    ZNB-1992-47b-0675 
 Volume    47 
111Author    Birgit Siewert, U. Lrich, M. ÜllerRequires cookie*
 Title    Die Kristallstrukturen von PPh4[AsCl4(TH F)2| und PPh4[AsBr4(THF)2]  
 Abstract    T he C rystal Structures o f P P h 4[A sCl4(T H F)2] and P P h 4[A sBr4(T H F)2] Tetraphenylphosphonium Tetrachloro-bis-tetrahydrofurane-arsenate(III), Tetraphenylphosphonium tetrabromo-bis-tetrahydrofurane-arsenate(III), Crystal Structure 
  Reference    Z. Naturforsch. 47b, 680—6 (1992); eingegangen am 14. Oktober 1991 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0680.pdf 
 Identifier    ZNB-1992-47b-0680 
 Volume    47 
112Author    Z. NaturforschRequires cookie*
 Title    Die Kristallstrukturen von N a2CoFeF7 und einer zweiten Modifikation von Na2CuFeF7: Eine weitere Weberit-Variante  
 Abstract    The Crystal Structures o f N a2C o F e F 7 an d a Second M odification o f N a 2C u F e F 7: A n o th e r W eberite V arian t M atth ias W elsch u n d D ietrich Babel* The monoclinic weberites N a2C oF eF 7 (a = 1262.2(10), b = 736.0(4), c = 2451.6(20) pm, ß = 99.71(5)°) and a second modification o f N a 2C uFeF 7 (a = 1244.4(2), b = 734.3(1), c = 2467.2(5) pm, ß = 99.27(3)°), crystallize isotypically in space group C 2 /c, Z = 16. The structure is an intermediate type between orthorhombic and trigonal weberites, characterized by pairs ofpar-allel chains o f octahedra [MF4F2/2]3' (M = Co, Cu) which run in turn along [110] and [110]. The average distances are F e -F = 192 pm in the [FeF6]3~ octahedra o f both compounds. C on­ siderable splitting o f distances occurs in the [CoF6]4-octahedra (av. C o -F = 201 pm), and by Jahn-Teller distortion even more in those o f [CuFJ4-(av. C u -F = 199 pm). One o f the copper surroundings is (pseudo)tetragonally elongated (av sual splitting into three long and three short bonds Some structural relations are discussed. 
  Reference    Z. Naturforsch. 47b, 685—6 (1992); eingegangen am 1. Oktober 1991 
  Published    1992 
  Keywords    Crystal Structure, Weberite, Heptafluorodimetallates(II, III), Jahn-Teller Distortion 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0685.pdf 
 Identifier    ZNB-1992-47b-0685 
 Volume    47 
113Author    Z. NaturforschRequires cookie*
 Title    Ruthenium(II)-Komplexe mit dem neuen Liganden (Oxetanyl-2-methyl)diphenylphosphan  
 Abstract    R uthenium (II) C om plexes w ith the N ovel L igand (O xetanyl-2-m ethyl)diphenylphosphine E k k eh ard Lindner* und A ndrea M öckel The new ether-phosphine ligand (oxetanyl-2-m ethyl)diphenylphosphine (1) with strongly basic properties is obtained by reaction o f LiPPh2 with 2-chlorom ethyloxetane. Reaction o f 1 with Cl2Ru(PPh3)3 results in the formation o f the bis(chelate) com plex rra«5-Cl2R u (P " 0)2 (2). (P —O = z/'-P-coordinated; P " 0 = ^2-0,P -eoordinated). With CO only one R u -O bond is cleaved to give the monocarbonylruthenium(II) complex rra«^-Cl2R u (C 0) (P ~ 0)(P " 0) (3). 3 shows fluxional behaviour only at higher temperatures as demonstrated by 3IP {'H } N M R spectra. 
  Reference    Z. Naturforsch. 47b, 693—6 (1992); eingegangen am 4. Dezember 1991 
  Published    1992 
  Keywords    Oxetanyl-Phosphine, O-Basicity, Ruthenium Complexes, Fluxional Behaviour 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0693.pdf 
 Identifier    ZNB-1992-47b-0693 
 Volume    47 
114Author    CarlD H, A. Ndreas, H. Eineb, D. Ietm, S. Talkeb, G. Eorge, M. SheldrickbRequires cookie*
 Title    Synthese und Eigenschaften von l  
 Abstract    Sulfurdiimides, 2,7,3,6-Tetrahydrobenzo[b]-l,2,7,3,6-thiadiazadiborepines, 1,2,4-Trithia-3,5-diborolanes, 2,5-D ihydrobenzo[b]-1,2,5-thiadiboroles 2,5-Bisdim ethylam ino-2,5-dihydrobenzo[b]-l,2,5-thiadiborole (2) has been obtained from the diiodine-derivative by reaction with dimethyl-aminotrimethylsilane. Reaction o f 2 or 2,5-bisdim ethylam ino-r,2'-dim ethyl-2,5-dihydrobenzo[b]-thiadiborole with di-rer/-butyl-, tert-butyl-trimethylsilyl-and bistrimethylsilyl-sulfurdiimide yields the 2,7,3,6-tetrahydrobenzo[b]-1,2,7,3,6-thiadiazadiborepines (3a-3e). 'H, "B, l3C N M R , MS and analytical data and results o f analysis are given. For 3 a the X-ray structure is reported. 
  Reference    Z. Naturforsch. 47b, 697—7 (1992); eingegangen am 24. Juni 1991 
  Published    1992 
  Keywords    2, 7, 3?6-Thiadiazadiborepinen, Kristallstruktur des 2, 7-Di-terf-butyl-3, 6-dimethyl-3, 6-dihydrobenzo-1, 2, 7, 3, 6-thiadiazadiborepins Syntheses and Properties o f 1, 2, 7, 3, 6-T hiadiazadiborepines, C rystal Structure o f 2, 7-D i-teT /-butyl-3, 6-dim ethyl-3, 6-dihydrobenzo-l, 2, 7, 3, 6-thiadiazadiborepin 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0697.pdf 
 Identifier    ZNB-1992-47b-0697 
 Volume    47 
115Author    A. Lfred, D. Bacher, Irin, Sens Und, U. Lrich, M. ÜllerRequires cookie*
 Title    Ein neuer Zugang zu Tetrathiooxalaten. Die Kristallstruktur von (NEt4)2[C2S4]  
 Abstract    (N E t4)2S5 was prepared from N E t4Cl and N a 2S4 in ethanol. Its reaction with boiling acetoni-trile yielded tetraethylammonium tetrathiooxalate. (N E t4)2[C2S4] was also obtained by heating (N E t4)2S5 with tetraethylammonium dithioacetate in ethanol. Benzyltriethylammonium tetra­ thiooxalate, (N E t3Bz)2[C2S4] • 2 toluene, crystallized after N E t3BzCl and N a 2S4 were heated in acetonitrile on subsequent addition o f toluene. The crystal structure o f (N E t4)2[C2S4] was de­ termined by X-ray diffraction (454 independent observed reflexions, R = 0.047). Crystal data: tetragonal, a = 871.2(1) pm, c = 1566.0(3) pm, space group P 4 2/nmc, Z = 2. The [C2S4]2-ion has point symmetry 4 m 2 (D 2d), i.e. the dihedral angle between the two CS2 groups is 90°. The ethyl groups o f the N E t4+ ions are disordered in two orientations. 
  Reference    Z. Naturforsch. 47b, 702 (1992); eingegangen am 21. Oktober 1991 
  Published    1992 
  Keywords    Tetraethylammoniun Pentasulfide, Tetraethylammonium Tetrathiooxalate, Benzyltriethylammonium Tetrathiooxalate, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0702.pdf 
 Identifier    ZNB-1992-47b-0702 
 Volume    47 
116Author    Z. NaturforschRequires cookie*
 Title    Synthese und Kristallstrukturen von  
 Abstract    Tris(glykolato)molybdän(VI) und T ris(pinakolato)molvbdän(VI) Syntheses and C rystal Structures o f T ris(glycolato)m olybdenum (V I) and T ris(pinacolato)m olybdenum (V I) Silke B uth, Sigrid W ocadlo, B ernhard N eum üller, F ra n k W eller und K u rt Dehnicke* PPh4[M oN (O Ph)4] has been prepared by reaction o f PPh4[M oN C l4] with sodium phenolate, as an orange-red crystal powder. The reactions o f glycole and pinacole, respectively, with M oN (0-r-B u)3 and M oN C 13, the latter in the presence o f a base, lead to the /rä-chelate com ­ plexes M o(O C 2H40) 3 and M o(OC:M e40) 3, respectively. The complexes were characterized by 'H and l3C N M R spectroscopy, the chelate complexes in addition by X-ray structure analysis. [Mo(OC-,H40) 3]: Space group P 2,/c, Z = 4, 2177 observed unique reflections. R = 0.047. Lattice dim ensions at -4 0 °C: a = 1168.3(2), b = 716.0(1), c = 1206.1(2) pm, ß = 92.84(1)°. [M o(OC2Me40) 3] • 2 C H 2C12: Space group Pbcn, Z = 4, 1860 observed unique reflections, R = 0.049. Lattice dimensions at -8 0 °C: a = 1772.3(1), b = 1023.8(1), c = 1600.0(2) pm. Both complexes form monomeric molecules, in which the molybdenum atom s are surround­ ed in a distorted octahedral fashion by the six oxygen atom s o f the chelates. 
  Reference    Z. Naturforsch. 47b, 706 (1992); eingegangen am 24. Oktober 1991 
  Published    1992 
  Keywords    Chelate Complexes o f M olybdenum, Synthesis, N M R Spectra, Crystal Structure 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0706.pdf 
 Identifier    ZNB-1992-47b-0706 
 Volume    47 
117Author    K. U. Rt, N. Iedenzu, Jo An, E. Serw, Atow Ska, Janusz Serw, Atow SkiRequires cookie*
 Title    Studies on l-Trimethylsilyl-2,4,6-triethylborazine and Related Species  
 Abstract    The unsymmetrically substituted borazine (C6H 5)3B3N 3H2[Si(CH3)3] has been obtained from the reaction o f C6H 5BC12 with HN [Si(C H 3)3]-,, and an improved synthesis o f (C2H 5)3B3N 3H 2[Si(CH3)3] has been developed. The reaction o f the latter with an excess o f BC13 proceeds with the ultimate formation o f Cl3B3N 3H 2[Si(CH3)3], whereas the reaction with one molar equivalent o f BBr3 leads to the formation o f Br(C2H5)2B3N 3H-,[Si(CH3)3], but which is contaminated by substantial am ounts o f Br(C2H 5)2B3N 3H3 besides a diborazinyl and additional products. C6H 5BBr2 reacts with N [Si(C H 3)3]3 to give the aminoborane [(CH3)3Si]2N BBr(C6H 5), but C6H5BC12 does not undergo a reaction under analogous condi­ tions. 
  Reference    Z. Naturforsch. 47b, 713—717 (1992); received September 12 1991 
  Published    1992 
  Keywords    Boron-Nitrogen Com pounds, Borazines, Unsymmetrically Substituted Borazines, Polyborazines 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0713.pdf 
 Identifier    ZNB-1992-47b-0713 
 Volume    47 
118Author    H. Arald, M. Üllerah, H. EinzRequires cookie*
 Title    Synthesis and Properties of Bis-(phenylenedithio)-tetrathiafulvalene (BPhDT-TTF): a New ;r-Donor for Organic Metals  
 Abstract    ritz3, R a lf N em etschekb, R u d o lf H ack lb, W erner B iberacherb, and C laus-P eter H eid m an n b The new 7r-donor bis-(phenylenedithio)-tetrathiafulvalene (5), synthesized via phosphite coupling o f 2-oxo-l,3-dithiolo-[4,5b][l,4]-benzodithiin (4), has been prepared in 5 steps start­ ing from 1,2-dimercaptobenzene and chloroacetyl chloride. Spectroscopic and electrochemical data point to a close similarity o f 5 and dibenzo-tetrathiafulvalene (D B -T TF). 5 forms a highly conducting radical-cation salt (crRT = 100 S/cm) with A sF fi" as counter ion. 
  Reference    Z. Naturforsch. 47b, 718 (1992); received December 23 1991 
  Published    1992 
  Keywords    Tetrathiafulvalene, Organic Metals, Electrocrystallization 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0718.pdf 
 Identifier    ZNB-1992-47b-0718 
 Volume    47 
119Author    Gerhard Hägele, Peter Reinemer3, Michael Batzb, DietrichM. OotzRequires cookie*
 Title    Kristallstruktur und molekulare Dynamik eines  
 Abstract    Stereoisomeren von (P,P,P",P"-Tetraphenyl)-l,l,2,2-ethan-tetrakisphosphinsäuretetraisopropylester Crystal Structure and M olecular Dynamics of a Stereoisomer of (P,P',P",P'"-Tetraphenyl)-l,l,2,2-ethane-tetraphosphinic Acid Tetraisopropylester The crystal and molecular structure o f (P,P',P",P"'-tetraphenyl)-1,1,2,2-ethane-tetraphos-phinic acid tetraisopropylester has been determined from single-crystal M oK a diffractometer data. The crystals are monoclinic with space group C2/c, Z = 4, a = 2054.5(9), b = 1189.8(5), c = 1800.8(8) pm, ß = 110.07(3)°. The structure was solved by direct methods and refined to R -0.046. A 250 ps-vacuo-trajectory was calculated using the Molecular Dynamics program G R O M O S. Structural data and M D results are compared to N M R spectroscopic data. A Karplus-type relation was confirmed for coupling constants 3ypp. 
  Reference    Z. Naturforsch. 47b, 725—7 (1992); eingegangen am 31. Juli 1991 
  Published    1992 
  Keywords    Crystal Structure, Conformation, Configuration, M D Analysis, N M R Spectra 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0725.pdf 
 Identifier    ZNB-1992-47b-0725 
 Volume    47 
120Author    Requires cookie*
 Title    Addition von Schwefeldioxid an Ruthenium-Thiolat-Komplexe, Struktur eines bemerkenswert stabilen T h iolat-S 02-Addukts [1]  
  Reference    Z. Naturforsch. 47b, 732 (1992) 
  Published    1992 
  Similar Items    Find
 DEBUG INFO      
 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-0732.pdf 
 Identifier    ZNB-1992-47b-0732 
 Volume    47 
Prev
...
6
7
8
9
10
...
Next