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  1. Article ; Online: Clayton W. Nuelle, M.D., Associate Editor, Arthroscopy Techniques.

    Lubowitz, James H

    Arthroscopy : the journal of arthroscopic & related surgery : official publication of the Arthroscopy Association of North America and the International Arthroscopy Association

    2020  Volume 36, Issue 1, Page(s) 6

    Language English
    Publishing date 2020-01-19
    Publishing country United States
    Document type Editorial
    ZDB-ID 632528-2
    ISSN 1526-3231 ; 0749-8063
    ISSN (online) 1526-3231
    ISSN 0749-8063
    DOI 10.1016/j.arthro.2019.10.029
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Letter regarding Ataman R, Thomas A, Roberge-Dao J, McKerral M, Auger C, Wittich W et al. Measurement Properties of the Mayo-Portland Adaptability Inventory (MPAI-4) and Related Measures: A Systematic Review. Arch Phys Med Rehabil 2023.

    Malec, James F

    Archives of physical medicine and rehabilitation

    2023  Volume 104, Issue 12, Page(s) 2169–2170

    MeSH term(s) Humans ; Brain Injuries ; Psychometrics
    Language English
    Publishing date 2023-09-14
    Publishing country United States
    Document type Letter ; Comment
    ZDB-ID 80057-0
    ISSN 1532-821X ; 0003-9993
    ISSN (online) 1532-821X
    ISSN 0003-9993
    DOI 10.1016/j.apmr.2023.06.025
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Element misidentification in X-ray crystallography: a reassessment of the [MCl2(diazadiene)] (M = Cr, Mo, W) series.

    Greene, Angelique F / Chandrasekaran, P / Yan, Yong / Mague, Joel T / Donahue, James P

    Inorganic chemistry

    2014  Volume 53, Issue 1, Page(s) 308–317

    Abstract: A series of reports describing the syntheses and structures of [MCl2(diazadiene)] (M = Cr, Mo, W ... the [MCl2(diazadiene)] (M = Mo, W) published structures reveals that the metal atoms were inappropriately ... electron [MCl2(diazadiene)] (M = Cr, Mo, W) complexes are in all cases the corresponding [ZnCl2(diazadiene ...

    Abstract A series of reports describing the syntheses and structures of [MCl2(diazadiene)] (M = Cr, Mo, W) complexes is reassessed in the context of known chemistry of low-valent Group VI metal complexes, crystallographic trends such as M-Cl bond lengths and unit cell volumes, and calculated metal-ligand bond lengths. Crystallographic data and computational results are inconsistent with any of these species being second or third row transition metal complexes. A review of the crystallographic information files accompanying the [MCl2(diazadiene)] (M = Mo, W) published structures reveals that the metal atoms were inappropriately treated with partial site occupancy factors (0.775 for Mo; 0.4005 and 0.417 for W), the effect of which was to manifest lighter-element behavior and better refinement in accord with the metal atoms' correct identity. A deliberate synthesis and characterization by X-ray diffraction of [ZnCl2((Mes)dad(Me))] ((Mes)dad(Me) = 1,4-bis(2,4,6-trimethylphenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene) are reported. Refinement of this structure with the same combination of second or third row metal and offsetting partial site occupancy is shown to provide final refinement statistics essentially the same as with the correct model employing M = Zn at site occupancy 1.00. Use of the published method for synthesis of [WCl2(diazadiene)] with (Mes)dad(Me) and [WBr4(MeCN)2] in lieu of [WCl4(MeCN)2] is shown to produce [ZnBr2((Mes)dad(Me))], which has also been characterized by X-ray diffraction. It is concluded that the unusual putative 12-electron [MCl2(diazadiene)] (M = Cr, Mo, W) complexes are in all cases the corresponding [ZnCl2(diazadiene)] complexes, Zn having been commonly employed as reducing agent in their synthesis.
    Language English
    Publishing date 2014-01-06
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1484438-2
    ISSN 1520-510X ; 0020-1669
    ISSN (online) 1520-510X
    ISSN 0020-1669
    DOI 10.1021/ic402246d
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Book ; Online: W. M.Gorman (1923 -2003)

    Honohan, Patrick / Neary, James Peter

    (CER working papers ; 03/21)

    2003  

    Institution Centre for Economic Research
    Author's details Patrick Honohan and J. Peter Neary
    Series title CER working papers ; 03/21
    Keywords 24#34#60#81
    Language English
    Size Online-Ressource, 21 p., text
    Edition [Elektronische Ressource]
    Publisher Centre for Economic Research
    Publishing place Dublin
    Document type Book ; Online
    Note IMD-Felder maschinell generiert
    Database ECONomics Information System

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  5. Article ; Online: Experimental and computational studies of binding of dinitrogen, nitriles, azides, diazoalkanes, pyridine, and pyrazines to M(PR(3))(2)(CO)(3) (M = Mo, W; R = Me, (i)Pr).

    Achord, Patrick / Fujita, Etsuko / Muckerman, James T / Scott, Brian / Fortman, George C / Temprado, Manuel / Cai, Xiaochen / Captain, Burjor / Isrow, Derek / Weir, John J / McDonough, James Eric / Hoff, Carl D

    Inorganic chemistry

    2009  Volume 48, Issue 16, Page(s) 7891–7904

    Abstract: ... i)Pr(3))(2)(CO)(3)(AdCN), W(P(i)Pr(3))(2)(CO)(3)(Me(2)NCN), W(P(i)Pr(3))(2)(CO)(3)(2,6-F(2)C(6)H(3)CN ... W(P(i)Pr(3))(2)(CO)(3)(2,4,6-Me(3)C(6)H(2)CN), W(P(i)Pr(3))(2)(CO)(3)(2,6-Me(2)pz), W(P(i)Pr(3))(2 ... CO)(3)(AdCN), Mo(P(i)Pr(3))(2)(CO)(3)(AdNC), and W(P(i)Pr(3))(2)(CO)(3)(AdNC) are reported. ...

    Abstract The enthalpies of binding of a number of N-donor ligands to the complex Mo(P(i)Pr(3))(2)(CO)(3) in toluene have been determined by solution calorimetry and equilibrium measurements. The measured binding enthalpies span a range of approximately 10 kcal mol(-1): DeltaH(binding) = -8.8 +/- 1.2 (N(2)-Mo(P(i)Pr(3))(2)(CO)(3)); -10.3 +/- 0.8 (N(2)); -11.2 +/- 0.4 (AdN(3) (Ad = 1-adamantyl)); -13.8 +/- 0.5 (N(2)CHSiMe(3)); -14.9 +/- 0.9 (pyrazine = pz); -14.8 +/- 0.6 (2,6-Me(2)pz); -15.5 +/- 1.8 (Me(2)NCN); -16.6 +/- 0.4 (CH(3)CN); -17.0 +/- 0.4 (pyridine); -17.5 +/- 0.8 ([4-CH(3)pz][PF(6)] (in tetrahydrofuran)); -17.6 +/- 0.4 (C(6)H(5)CN); -18.6 +/- 1.8 (N(2)CHC( horizontal lineO)OEt); and -19.3 +/- 2.5 kcal mol(-1) (pz)Mo(P(i)Pr(3))(2)(CO)(3)). The value for the isonitrile AdNC (-29.0 +/- 0.3) is 12.3 kcal mol(-1) more exothermic than that of the nitrile AdCN (-16.7 +/- 0.6 kcal mol(-1)). The enthalpies of binding of a range of arene nitrile ligands were also studied, and remarkably, most nitrile complexes were clustered within a 1 kcal mol(-1) range despite dramatic color changes and variation of nu(CN). Computed structural and spectroscopic parameters for the complexes Mo(P(i)Pr(3))(2)(CO)(3)L are in good agreement with experimental data. Computed binding enthalpies for Mo(P(i)Pr(3))(2)(CO)(3)L exhibit considerable scatter and are generally smaller compared to the experimental values, but relative agreement is reasonable. Computed enthalpies of binding using a larger basis set for Mo(PMe(3))(2)(CO)(3)L show a better fit to experimental data than that for Mo(P(i)Pr(3))(2)(CO)(3)L using a smaller basis set. Crystal structures of Mo(P(i)Pr(3))(2)(CO)(3)(AdCN), W(P(i)Pr(3))(2)(CO)(3)(Me(2)NCN), W(P(i)Pr(3))(2)(CO)(3)(2,6-F(2)C(6)H(3)CN), W(P(i)Pr(3))(2)(CO)(3)(2,4,6-Me(3)C(6)H(2)CN), W(P(i)Pr(3))(2)(CO)(3)(2,6-Me(2)pz), W(P(i)Pr(3))(2)(CO)(3)(AdCN), Mo(P(i)Pr(3))(2)(CO)(3)(AdNC), and W(P(i)Pr(3))(2)(CO)(3)(AdNC) are reported.
    Language English
    Publishing date 2009-08-17
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1484438-2
    ISSN 1520-510X ; 0020-1669
    ISSN (online) 1520-510X
    ISSN 0020-1669
    DOI 10.1021/ic900764e
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Gynecologic oncology 2005: What it "oughta" be! Presented to Society of Gynecologic Oncologists, Miami Beach, Florida, USA, by James W. Orr, Jr., M.D.

    Orr, James W

    Gynecologic oncology

    2005  Volume 98, Issue 3, Page(s) 344–352

    MeSH term(s) Female ; Gynecology/education ; Gynecology/methods ; Gynecology/standards ; Humans ; Medical Oncology/education ; Medical Oncology/methods ; Medical Oncology/standards ; Societies, Medical
    Language English
    Publishing date 2005-09
    Publishing country United States
    Document type Addresses ; Editorial
    ZDB-ID 801461-9
    ISSN 1095-6859 ; 0090-8258
    ISSN (online) 1095-6859
    ISSN 0090-8258
    DOI 10.1016/j.ygyno.2005.07.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Rapid Inversion at Phosphorus in the [eta(4)-(C(6)H(11))(3)SnP(7)W(CO)(3)](2)(-) and [(en)(CO)(3)W(eta(1),eta(4)-P(7))M(CO)(3)](3)(-) Ions Where M = Cr, W.

    Charles, Scott / Danis, Janet A. / Fettinger, James C. / Eichhorn, Bryan W.

    Inorganic chemistry

    1997  Volume 36, Issue 17, Page(s) 3772–3778

    Abstract: Ethylenediamine (en) solutions of [eta(4)-P(7)M(CO)(3)](3)(-) ions [M = Cr (1a), W (1b)] react ... with (mesitylene)W(CO)(3) to form the bimetallic complexes [(en)(CO)(3)W(eta(1),eta(4)-P(7))M(CO)(3)](3)(-) where M ... Cr (3a), W (3b) in good yield. Compound 3b can be prepared directly from P(7)(3)(-) and 2 equiv ...

    Abstract Ethylenediamine (en) solutions of [eta(4)-P(7)M(CO)(3)](3)(-) ions [M = Cr (1a), W (1b)] react with (mesitylene)W(CO)(3) to form the bimetallic complexes [(en)(CO)(3)W(eta(1),eta(4)-P(7))M(CO)(3)](3)(-) where M = Cr (3a), W (3b) in good yield. Compound 3b can be prepared directly from P(7)(3)(-) and 2 equiv of (mesitylene)W(CO)(3). Compound 3a reacts with 1 equiv of P(7)(3)(-) to form 1a and 1b. En solutions of 1b react with 1 equiv of (C(6)H(11))(3)SnCl to give [eta(4)-(C(6)H(11))(3)SnP(7)W(CO)(3)](2)(-) (4) in good crystalline yield as the [K(2,2,2-crypt)](+) salt. The X-ray structure of the [K(2,2,2-crypt)](+) salt 3b revealed a norbornadiene-like P(7) cage bound eta(4) to the W(CO)(3) fragment (cf. [eta(4)-P(7)W(CO)(3)](3)(-)) and eta(1) to the (en)(CO)(3)W fragment via the long W(2)-P(1) bond of 2.643(3) Å. The structure of 4 is similar, with a (C(6)H(11))(3)Sn(+) group attached to the P(1) atom of the [eta(4)-P(7)W(CO)(3)](3)(-) complex. The coordination geometry at P(1) is distinctly pyramidal in both compounds, which leaves the ions with no crystallographic symmetry. For complexes 3a and 3b, two fluxional processes are rapid on the NMR time scale at -50 degrees C (202 MHz) that give the P(7) cages virtual C(2)(v)() symmetry in solution and AA'A"A"'MM"X spin systems. These processes are (1) a wagging of the four P atoms bound to the M(CO)(3) units and (2) rapid inversion at P(1). For 4, inversion at phosphorus becomes slow on the NMR time scale at low temperature (-50 degrees C, 83 MHz) with DeltaG() = 13 kcal/mol. Crystallographic data are as follows. [K(2,2,2-crypt)](3)3b.en: triclinic, P&onemacr;, a = 14.396(4) Å, b = 17.543(3) Å, c = 20.518(2) Å, alpha = 82.419(11) degrees, beta = 76.830(14) degrees, gamma = 69.16(2) degrees, V = 4708(2) Å(3), Z = 2, R(F) = 5.52%, R(w)(F(2)) = 14.31%. [K(2,2,2-crypt)](2)4: triclinic, P&onemacr;, a = 12.247(2) Å, b = 15.1909(14) Å, c = 21.292(3) Å, alpha = 97.374(10) degrees, beta = 93.273(13) degrees, gamma = 111.217(9) degrees, V = 3639.8(8) Å(3), Z = 2, R(F) = 10.50%, R(w)(F(2)) = 20.21%.
    Language English
    Publishing date 1997-08-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1484438-2
    ISSN 1520-510X ; 0020-1669
    ISSN (online) 1520-510X
    ISSN 0020-1669
    DOI 10.1021/ic961177q
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Book ; Online ; E-Book: Basics of musculoskeletal ultrasound

    Daniels, James M. / Dexter, William W.

    2021  

    Author's details James M. Daniels, William W Dexter editors
    Keywords Electronic books
    Language English
    Size 1 Online-Ressource (xii, 286 Seiten)
    Edition Second edition
    Publisher Springer
    Publishing place Cham
    Publishing country Switzerland
    Document type Book ; Online ; E-Book
    Note Description based on publisher supplied metadata and other sources
    Remark Zugriff für angemeldete ZB MED-Nutzerinnen und -Nutzer
    HBZ-ID HT021016731
    ISBN 978-3-030-73906-5 ; 9783030739058 ; 3-030-73906-6 ; 3030739058
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  9. Article ; Online: Synthesis, Structure, and Reactivities of [eta(2)-P(7)M(CO)(4)](3)(-), [eta(2)-HP(7)M(CO)(4)](2)(-), and [eta(2)-RP(7)M(CO)(4)](2)(-) Zintl Ion Complexes Where M = Mo, W.

    Charles, Scott / Fettinger, James C. / Eichhorn, Bryan W.

    Inorganic chemistry

    1996  Volume 35, Issue 6, Page(s) 1540–1548

    Abstract: Ethylenediamine (en) solutions of [eta(4)-P(7)M(CO)(3)](3)(-) ions [M = W (1a), Mo (1b)] react ... complexes [M = W (4a), Mo (4b)]. Compounds 4 are unstable, losing CO to re-form 1, but are highly ... under one atmosphere of CO to form microcrystalline yellow powders of [eta(2)-P(7)M(CO)(4)](3 ...

    Abstract Ethylenediamine (en) solutions of [eta(4)-P(7)M(CO)(3)](3)(-) ions [M = W (1a), Mo (1b)] react under one atmosphere of CO to form microcrystalline yellow powders of [eta(2)-P(7)M(CO)(4)](3)(-) complexes [M = W (4a), Mo (4b)]. Compounds 4 are unstable, losing CO to re-form 1, but are highly nucleophilic and basic. They are protonated with methanol in en solvent giving [eta(2)-HP(7)M(CO)(4)](2)(-) ions (5) and are alkylated with R(4)N(+) salts in en solutions to give [eta(2)-RP(7)M(CO)(4)](2)(-) complexes (6) in good yields (R = alkyl). Compounds 5 and 6 can also be prepared by carbonylations of the [eta(4)-HP(7)M(CO)(3)](2)(-) (3) and [eta(4)-RP(7)M(CO)(3)](2)(-) (2) precursors, respectively. The carbonylations of 1-3 to form 4-6 require a change from eta(4)- to eta(2)-coordination of the P(7) cages in order to maintain 18-electron configurations at the metal centers. Comparative protonation/deprotonation studies show 4 to be more basic than 1. The compounds were characterized by IR and (1)H, (13)C, and (31)P NMR spectroscopic studies and microanalysis where appropriate. The [K(2,2,2-crypt)](+) salts of 5 were characterized by single crystal X-ray diffraction. For 5, the M-P bonds are very long (2.71(1) Å, average). The P(7)(3)(-) cages of 5 are not displaced by dppe. The P(7) cages in 4-6 have nortricyclane-like structures in contrast to the norbornadiene-type geometries observed for 1-3. (31)P NMR spectroscopic studies for 5-6 show C(1) symmetry in solution (seven inequivalent phosphorus nuclei), consistent with the structural studies for 5, and C(s)() symmetry for 4 (five phosphorus nuclei in a 2:2:1:1:1 ratio). Crystallographic data for [K(2,2,2-crypt)](2)[eta(2)-HP(7)W(CO)(4)].en: monoclinic, space group C2/c, a = 23.067(20) Å, b = 12.6931(13) Å, c = 21.433(2) Å, beta = 90.758(7) degrees, V = 6274.9(10) Å(3), Z = 4, R(F) = 0.0573, R(w)(F(2)) = 0.1409. For [K(2,2,2-crypt)](2)[eta(2)-HP(7)Mo(CO)(4)].en: monoclinic, space group C2/c, a = 22.848(2) Å, b = 12.528(2) Å, c = 21.460(2) Å, beta = 91.412(12) degrees, V = 6140.9(12) Å(3), Z = 4, R(F) = 0.0681, R(w)(F(2)) = 0.1399.
    Language English
    Publishing date 1996-03-13
    Publishing country United States
    Document type Journal Article
    ZDB-ID 1484438-2
    ISSN 1520-510X ; 0020-1669
    ISSN (online) 1520-510X
    ISSN 0020-1669
    DOI 10.1021/ic9511534
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Book ; Conference proceedings ; Online: (Table T1) Paleomagnetic characterization of ODP Hole 198-1213B basalts, supplementary data to: Tominaga, M; Sager, William W; Channell, James ET (2005): Paleomagnetism of the igneous section, Hole 1213B, Shatsky Rise. In: Bralower, TJ; Premoli Silva, I; Malone, MJ (eds.) Proceedings of the Ocean Drilling Program, Scientific Results, College Station, TX (Ocean Drilling Program), 198, 1-15

    Tominaga, M / Channell, James ET / Sager, William W

    2005  

    Abstract: Paleomagnetic measurements were made on 52 samples from the igneous section of Ocean Drilling Program Hole 1213B for the purpose of determining paleoinclination and polarity and giving insight about volcanic emplacement. Samples were taken at ... ...

    Abstract Paleomagnetic measurements were made on 52 samples from the igneous section of Ocean Drilling Program Hole 1213B for the purpose of determining paleoinclination and polarity and giving insight about volcanic emplacement. Samples were taken at approximately even intervals from the three basaltic sills that make up the section, and all samples were demagnetized using an alternating field or thermal methods in an effort to determine the characteristic magnetization direction. Half of the samples gave inconsistent results. Furthermore, natural remanent magnetization values were strong and median destructive field values were low, implying that the basalts are prone to acquiring an overprint from the drill string. In addition, hysteresis results show low coercivities and lie in the pseudosingle-domain field of a Day plot (Mr/Ms vs. Bcr/Bc). All of these observations suggest that the samples are characterized by a low-coercivity magnetic mineral, such as titanomagnetite, that may not always preserve a stable characteristic remanence. Nevertheless, 26 samples produced consistent inclinations, giving shallow, negative values that are considered the likely characteristic direction. There is no statistical difference between mean inclinations for the three units, implying they erupted within a short time. Measurements from all reliable samples were averaged to give a paleoinclination of -9.3° with 95% confidence limits from -41.8° to 27.5°, the large uncertainty resulting from the fact that paleosecular variation is not averaged. Although the large uncertainty makes a unique assignment of polarity difficult, the interpretation that is most consistent with other Pacific paleomagnetic data is that the magnetization has a reversed polarity acquired slightly north of the equator.
    Language English
    Dates of publication 2005-9999
    Size Online-Ressource
    Publisher PANGAEA - Data Publisher for Earth & Environmental Science
    Publishing place Bremen/Bremerhaven
    Document type Book ; Conference proceedings ; Online
    Note This dataset is supplement to doi:10.2973/odp.proc.sr.198.113.2005
    DOI 10.1594/PANGAEA.778245
    Database Library catalogue of the German National Library of Science and Technology (TIB), Hannover

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