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  • 1
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  Angewandte Chemie Vol. 131, No. 16 ( 2019-04-08), p. 5506-5511
    In: Angewandte Chemie, Wiley, Vol. 131, No. 16 ( 2019-04-08), p. 5506-5511
    Abstract: Ausgehend von Fluoridosilikat‐Vorstufen in reinem Cyantrimethylsilan, Me 3 Si‐CN, wurde eine Reihe verschiedener Ammoniumsalze [R 3 NMe] + (R=Et, n Pr, n Bu) mit den neuen [SiF(CN) 5 ] 2− ‐ und [Si(CN) 6 ] 2− ‐Dianionen in einfachen, temperaturgesteuerten F − /CN − ‐Austauschreaktionen synthetisiert. Mit zersetzbaren, nicht‐unschuldigen Kationen wie [R 3 NH] + konnten Metallsalze des Typs M 2 [Si(CN) 6 ] (M + =Li + , K + ) durch Neutralisationsreaktionen mit entsprechenden Metallhydroxiden hergestellt werden. Die ionische Flüssigkeit [BMIm] 2 [Si(CN) 6 ] (Schmp.=72 °C) wurde durch eine Salzmetathesereaktion erhalten. Alle synthetisierten Salze konnten in guten Ausbeuten isoliert und vollständig charakterisiert werden.
    Type of Medium: Online Resource
    ISSN: 0044-8249 , 1521-3757
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2019
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    detail.hit.zdb_id: 505872-7
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    detail.hit.zdb_id: 505867-3
    detail.hit.zdb_id: 506259-7
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  • 2
    Online Resource
    Online Resource
    Wiley ; 2020
    In:  Angewandte Chemie International Edition Vol. 59, No. 26 ( 2020-06-22), p. 10508-10513
    In: Angewandte Chemie International Edition, Wiley, Vol. 59, No. 26 ( 2020-06-22), p. 10508-10513
    Abstract: Although pure hydrogen cyanide can spontaneously polymerize or even explode, when initiated by small amounts of bases (e.g. CN − ), the reaction of liquid HCN with [WCC]CN (WCC=weakly coordinating cation=Ph 4 P, Ph 3 PNPPh 3 =PNP) was investigated. Depending on the cation, it was possible to extract salts containing the formal dihydrogen tricyanide [CN(HCN) 2 ] − and trihydrogen tetracyanide ions [CN(HCN) 3 ] − from liquid HCN when a fast crystallization was carried out at low temperatures. X‐ray structure elucidation revealed hydrogen‐bridged linear [CN(HCN) 2 ] − and Y‐shaped [CN(HCN) 3 ] − molecular ions in the crystal. Both anions can be considered members of highly labile cyanide‐HCN solvates of the type [CN(HCN) n ] − ( n= 1, 2, 3 …) as well as formal polypseudohalide ions.
    Type of Medium: Online Resource
    ISSN: 1433-7851 , 1521-3773
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 2011836-3
    detail.hit.zdb_id: 123227-7
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  • 3
    Online Resource
    Online Resource
    Ovid Technologies (Wolters Kluwer Health) ; 2010
    In:  Anesthesia & Analgesia Vol. 110, No. 5 ( 2010-05), p. 1448-1456
    In: Anesthesia & Analgesia, Ovid Technologies (Wolters Kluwer Health), Vol. 110, No. 5 ( 2010-05), p. 1448-1456
    Type of Medium: Online Resource
    ISSN: 0003-2999
    RVK:
    Language: English
    Publisher: Ovid Technologies (Wolters Kluwer Health)
    Publication Date: 2010
    detail.hit.zdb_id: 2018275-2
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  • 4
    In: JMIR Serious Games, JMIR Publications Inc., Vol. 10, No. 4 ( 2022-12-13), p. e36197-
    Abstract: The wide availability of mobile phones has made it easy to disseminate health-related information and make it accessible. With gamification, mobile apps can nudge people to make informed health choices, including attending cervical cancer screening. Objective This matched retrospective cohort study examined the association between exposure to the FightHPV mobile app gamified educational content and having a cervical exam in the following year. Methods Women aged 20 to 69 years who signed an electronic consent form after downloading the FightHPV app in 2017 (intervention group) were matched 1:6 with women of the same age and with the same screening history (reference group) in 2015. To estimate the impact of exposure to the FightHPV app, we estimated cumulative incidence and hazard ratios (HRs) with 95% CIs. We used data from the Norwegian Cervical Cancer Screening Program database and Statistics Norway to determine screening participation and outcomes, respectively. Results We matched 3860 women in the control group to 658 women in the intervention group; 6 months after enrollment, 29.6% (195/658) of the women in the intervention group and 15.21% (587/3860) of those in the reference group underwent a cervical exam (P 〈 .01). Women exposed to the FightHPV app were 2 times more likely to attend screening (adjusted HR 2.3, 95% CI 2.0-2.7), during which they were 13 times more likely to be diagnosed with high-grade abnormality (adjusted HR 12.7, 95% CI 5.0-32.5) than the women in the reference group. Conclusions Exposure to the FightHPV app significantly increased cervical cancer screening attendance across the various analyses and improved detection of women with high risk for cervical cancer. For the first time, we demonstrated the effectiveness of gamification combined with mobile technology in cancer prevention by empowering women to make active health-related decisions. Gamification can significantly improve the understanding of complicated scientific concepts behind interventions and increase the acceptance of proposed cancer control measures.
    Type of Medium: Online Resource
    ISSN: 2291-9279
    Language: English
    Publisher: JMIR Publications Inc.
    Publication Date: 2022
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  • 5
    In: Dalton Transactions, Royal Society of Chemistry (RSC), Vol. 49, No. 39 ( 2020), p. 13655-13662
    Type of Medium: Online Resource
    ISSN: 1477-9226 , 1477-9234
    Language: English
    Publisher: Royal Society of Chemistry (RSC)
    Publication Date: 2020
    detail.hit.zdb_id: 1472887-4
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  • 6
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  Zeitschrift für anorganische und allgemeine Chemie Vol. 645, No. 12 ( 2019-06-28), p. 835-839
    In: Zeitschrift für anorganische und allgemeine Chemie, Wiley, Vol. 645, No. 12 ( 2019-06-28), p. 835-839
    Abstract: Several pseudohalide containing ionic liquids with quarternary ammonium counter cations of the general formula [ R 3 MeN]X [ R = ethyl ( 1X ), n ‐butyl ( 2X ) with X – = CN – , N 3 – , OCN – , and SCN – ] were synthesized by decomposition of the corresponding trialkylammonium methylcarbonate in the reaction with Me 3 Si– X . We also treated 2CN with OP(OMe) 3 , yielding [ n Bu 3 MeN][O 2 P(OMe) 2 ] and acetonitrile (Me‐CN). The double salt [ n Bu 3 MeN] 2 {[B(OMe) 3 (CN)](CN)} was obtained from the reaction of 2CN with B(OMe) 3 , featuring the formation of the monocyanotrimethoxyborate anion, [B(OMe) 3 (CN)] – , co‐crystallized with [ n Bu 3 MeN]CN. [ n Bu 3 MeN] 2 {[B(OMe) 3 (CN)](CN)} was fully characterized including structure elucidation.
    Type of Medium: Online Resource
    ISSN: 0044-2313 , 1521-3749
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 201094-X
    detail.hit.zdb_id: 1481139-X
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  • 7
    Online Resource
    Online Resource
    Wiley ; 2020
    In:  Angewandte Chemie Vol. 132, No. 26 ( 2020-06-22), p. 10594-10599
    In: Angewandte Chemie, Wiley, Vol. 132, No. 26 ( 2020-06-22), p. 10594-10599
    Abstract: Obwohl reiner Cyanwasserstoff spontan polymerisieren oder sogar explodieren kann, was durch geringe Mengen an Basen (z. B. CN − ) ausgelöst wird, wurde die Reaktion von flüssigem HCN mit [WCC]CN (WCC=schwach koordinierendes Kation=Ph 4 P, Ph 3 PNPPh 3 =PNP) untersucht. Abhängig vom Kation konnten aus flüssigem HCN Salze, welche die formalen Dihydrogentricyanid‐ [CN(HCN) 2 ] − und Trihydrogentetracyanid‐Ionen [CN(HCN) 3 ] − enthalten, isoliert werden, wenn die Kristallisation schnell und bei niedrigen Temperaturen durchgeführt wurde. Die Röntgenstrukturaufklärung ergab wasserstoffverbrückte lineare [CN(HCN) 2 ] − und Y‐förmige [CN(HCN) 3 ] − Molekülionen im Kristall. Beide Anionen können als Vertreter hochlabiler Cyanid‐HCN‐Solvate vom Typ [CN(HCN) n ] − ( n =1, 2, 3…) sowie als formale Polypseudohalogenidionen betrachtet werden.
    Type of Medium: Online Resource
    ISSN: 0044-8249 , 1521-3757
    URL: Issue
    RVK:
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 505868-5
    detail.hit.zdb_id: 506609-8
    detail.hit.zdb_id: 514305-6
    detail.hit.zdb_id: 505872-7
    detail.hit.zdb_id: 1479266-7
    detail.hit.zdb_id: 505867-3
    detail.hit.zdb_id: 506259-7
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  • 8
    Online Resource
    Online Resource
    Wiley ; 2020
    In:  European Journal of Inorganic Chemistry Vol. 2020, No. 25 ( 2020-07-07), p. 2457-2464
    In: European Journal of Inorganic Chemistry, Wiley, Vol. 2020, No. 25 ( 2020-07-07), p. 2457-2464
    Abstract: Functionalized imidazolium cations were combined with the hexacyanidosilicate anion, [Si(CN) 6 ] 2– , by salt metathesis reactions with K 2 [Si(CN) 6 ], yielding novel ionic compounds of the general formula [R–Ph( n Bu)Im] 2 [Si(CN) 6 ] {R = 2‐Me ( 1 ), 4‐Me ( 2 ), 2,4,6‐Me = Mes ( 3 ), 2‐MeO ( 4 ), 2,4‐F ( 5 ), 4‐Br ( 6 ); Im = imidazolium}. All synthesized imidazolium hexacyanidosilicates decompose upon thermal treatment above 95 °C (96 – 164 °C). Furthermore, the hexa‐borane‐adduct [Mes( n Bu)Im] 2 {Si[(CN)B(C 6 F 5 ) 3 ] 6 } · 6CH 2 Cl 2 ( 7 ), which is thermally stable up to 215 °C, was obtained from the reaction of 3 with Lewis acidic B(C 6 F 5 ) 3 . In CH 3 CN solution, decomposition of the hexaadduct to the Lewis‐acid‐base adduct CH 3 CN–B(C 6 F 5 ) 3 and [(C 6 F 5 ) 3 B · ( µ ‐CN) · B(C 6 F 5 ) 3 ] – was observed. All synthesized compounds were isolated in good yields and were completely characterized including single crystal structure elucidations.
    Type of Medium: Online Resource
    ISSN: 1434-1948 , 1099-0682
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2020
    detail.hit.zdb_id: 1475009-0
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  • 9
    Online Resource
    Online Resource
    Wiley ; 2019
    In:  Angewandte Chemie International Edition Vol. 58, No. 16 ( 2019-04-08), p. 5452-5456
    In: Angewandte Chemie International Edition, Wiley, Vol. 58, No. 16 ( 2019-04-08), p. 5452-5456
    Abstract: Starting from fluoridosilicate precursors in neat cyanotrimethylsilane, Me 3 Si−CN, a series of different ammonium salts [R 3 NMe] + (R=Et, n Pr, n Bu) with the novel [SiF(CN) 5 ] 2− and [Si(CN) 6 ] 2− dianions was synthesized in facile, temperature controlled F − /CN − exchange reactions. Utilizing decomposable, non‐innocent cations, such as [R 3 NH] + , it was possible to generate metal salts of the type M 2 [Si(CN) 6 ] (M + =Li + , K + ) via neutralization reactions with the corresponding metal hydroxides. The ionic liquid [BMIm] 2 [Si(CN) 6 ] (m.p.=72 °C, BMIm=1‐butyl‐3‐methylimidazolium) was obtained by a salt metathesis reaction. All the synthesized salts could be isolated in good yields and were fully characterized.
    Type of Medium: Online Resource
    ISSN: 1433-7851 , 1521-3773
    URL: Issue
    RVK:
    Language: English
    Publisher: Wiley
    Publication Date: 2019
    detail.hit.zdb_id: 2011836-3
    detail.hit.zdb_id: 123227-7
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  • 10
    In: ChemistryOpen, Wiley, Vol. 10, No. 2 ( 2021-02), p. 62-71
    Abstract: Within the second funding period of the SPP 1708 “Material Synthesis near Room Temperature”,which started in 2017, we were able to synthesize novel anionic species utilizing Ionic Liquids (ILs) both, as reaction media and reactant. ILs, bearing the decomposable and non‐innocent methyl carbonate anion [CO 3 Me] − , served as starting material and enabled facile access to pseudohalide salts by reaction with Me 3 Si−X (X=CN, N 3 , OCN, SCN). Starting with the synthesized Room temperature Ionic Liquid (RT‐IL) [ n Bu 3 MeN][B(OMe) 3 (CN)], we were able to crystallize the double salt [ n Bu 3 MeN] 2 [B(OMe) 3 (CN)](CN). Furthermore, we studied the reaction of [WCC] SCN and [WCC]CN (WCC=weakly coordinating cation) with their corresponding protic acids HX (X=SCN, CN), which resulted in formation of [H(NCS) 2 ] − and the temperature labile solvate anions [CN(HCN) n ] − ( n =2, 3). In addition, the highly labile anionic HCN solvates were obtained from [PPN]X ([PPN] =μ‐nitridobis(triphenylphosphonium), X=N 3 , OCN, SCN and OCP) and HCN. Crystals of [PPN][X(HCN) 3 ] (X=N 3 , OCN) and [PPN][SCN(HCN) 2 ] were obtained when the crystallization was carried out at low temperatures. Interestingly, reaction of [PPN] OCP with HCN was noticed, which led to the formation of [P(CN) 2 ] − , crystallizing as HCN disolvate [PPN][P(CN⋅HCN) 2 ]. Furthermore, we were able to isolate the novel cyanido(halido) silicate dianions of the type [SiCl 0.78 (CN) 5.22 ] 2− and [SiF(CN) 5 ] 2− and the hexa‐substituted [Si(CN) 6 ] 2− by temperature controlled halide/cyanide exchange reactions. By facile neutralization reactions with the non‐innocent cation of [Et 3 HN] 2 [Si(CN) 6 ] with MOH (M=Li, K), Li 2 [Si(CN) 6 ] ⋅ 2 H 2 O and K 2 [Si(CN) 6 ] were obtained, which form three dimensional coordination polymers. From salt metathesis processes of M 2 [Si(CN) 6 ] with different imidazolium bromides, we were able to isolate new imidazolium salts and the ionic liquid [BMIm] 2 [Si(CN) 6 ]. When reacting [Mes( n Bu)Im] 2 [Si(CN) 6 ] with an excess of the strong Lewis acid B(C 6 F 5 ) 3 , the voluminous adduct anion {Si[CN⋅B(C 6 F 5 ) 3 ] 6 } 2− was obtained.
    Type of Medium: Online Resource
    ISSN: 2191-1363 , 2191-1363
    URL: Issue
    Language: English
    Publisher: Wiley
    Publication Date: 2021
    detail.hit.zdb_id: 2655605-4
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