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2.146 Treffer

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  1. Detailansicht für Treffer 1 öffnen
    Molecular engineering of 3-arylated tetrazo[1,2-b]indazoles: divergent synthesis and structure–property relationships.
    Bousfiha, Asmae ; Abidi, Oumaima ; et al.
    In: Dalton Transactions: An International Journal of Inorganic Chemistry, Jg. 53 (2024-07-07), Heft 25, S. 10737-10743
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  2. Detailansicht für Treffer 2 öffnen
    Increasing the electron donation in a dinucleating ligand family: molecular and electronic structures in a series of Co<superscript>II</superscript>Co<superscript>II</superscript> complexes.
    Depenbrock, Felix ; Limpke, Thomas ; et al.
    In: Dalton Transactions: An International Journal of Inorganic Chemistry, Jg. 53 (2024-06-14), Heft 22, S. 9554-9567
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  3. Detailansicht für Treffer 3 öffnen
    Gd(iii) complex of a monophosphinate-bis(phosphonate) DOTA analogue with a high relaxivity; Lanthanide(iii) complexes for imaging and radiotherapy of calcified tissuesElectronic supplementary information (ESI) available: Complexation of the DO3APBPmonitored by 31P{1H} NMR; 31P{1H}, 1H NMR spectra of Ln-DO3APBPcomplexes; 31P{1H} NMR spectra of Eu- and Yb-DO3APBPcomplexes at different temperatures; 31P{1H} NMR titration curves of SA and TSA species in the Yb-DO3APBPcomplex and distribution diagrams; pH dependence of the relaxivity; the temperature dependence of reduced 17O NMR chemical shifts, R1, R2, and 1H NMRD profiles of the Gd-DO3APBPcomplex at pH = 6; τRas a function of concentration of the La-DO3APBPcomplex; kinetic stability of the Eu-DO3APBPcomplex against transmetallation tested by luminescence measurements; paramagnetic contribution to 1H NMRD profiles of the Gd(iii) complexes of the ligands DO3APBP, BPAMD, BPAPD upon adsorption on HA; the geometrical parameters found in the c
    Vitha, Tomáš ; Kubíek, Vojtch ; et al.
    In: Dalton Transactions: An International Journal of Inorganic Chemistry, Jg. 2009 (2009-04-13), Heft 17, S. 3204-3214
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  4. Detailansicht für Treffer 4 öffnen
    Highly selective and sensitive fluorescent "TURN-ON" furan-based Schiff base for zinc(II) ion probing: chemical synthesis, DFT studies, and X-ray crystal structure.
    N. R., Divyashree ; Revanasiddappa, Hosakere D. ; et al.
    In: New Journal of Chemistry, Jg. 47 (2023-10-07), Heft 37, S. 17420-17433
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  5. Detailansicht für Treffer 5 öffnen
    1D → 1D Two-fold parallel interpenetrated coordination polymers with a bis(pyridylurea) ligandElectronic supplementary information (ESI) available: Experimental details: synthesis and characterization of the ligand L and compounds 1–4, and crystallographic data. CCDC reference numbers 739485–739488. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b922566hCrystal data for 1: C30H52CdCl2N12O12(956.14), colourless block, crystal system: orthorhombic, space group: Ibam, a= 14.1957(10), b= 15.7796 (11), c= 18.5297(12) Å, V= 4150.7(5) Å3, T= 173(2) K, Z= 4, Dc= 1.530 g cm−3, F000= 1976, μ= 0.726 mm−1, 13087 reflections collected, 1894 unique (Rint= 0.024), 1744 observed [I> 2σ(I)]; R1= 0.043, wR2= 0.121 [I> 2σ(I)].Crystal data for 2: C30H40CdN14O12(901.16), colourless block, crystal system: orthorhombic, space group: Ibam, a= 14.2829(14), b= 15.3547(15), c= 18.6193(18) Å, V= 4083.4(7) Å3, T= 173(2) K, Z= 4, Dc= 1.466 g cm−3, F000= 1848, μ= 0.609 mm−1, 140
    Li, Shaoguang ; Wu, Biao ; et al.
    In: CrystEngComm, Jg. 12 (2010-07-01), Heft 7, S. 2001-2004
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  6. Detailansicht für Treffer 6 öffnen
    A simple peptidomimetic that self-associates on the solid state to form a nanoporous architecture containing chiral π-channelsElectronic supplementary information (ESI) available: Crystal data for 4c. CCDC reference numbers 279709, 738995and 739838. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b922172gCrystallographic data for compound 4a(CCDC-279709): C20H26N4O2. 1/3C4H10O, M= 379.15, hexagonal, a= 16.994(2) Å, c= 6.2966(7) Å, V= 1574.8(3) Å3, T= 173 K, space group P64(No. 172), Z= 3, 14595 reflections measured, 2348 unique (Rint= 0.028) which were used in all calculations. Final wR2= 0.0853 and R1= 0.0348 for data with I> 2σ(I). Due to the absence of anomalous scatterers, Friedel pairs were merged. Compound 4a′ (CCDC-739838): C20H26N4O2·1/2CH2Cl2, M= 396.91, hexagonal, a= 16.9390(10) Å, c= 6.2865(5) Å, V= 1562.12(18) Å3, T= 173 K, space group P64(No. 172), Z= 3, 15134 reflections measured, 2305 unique (Rint= 0.061) which were used in all calcul
    Becerril, Jorge ; Bolte, Michael ; et al.
    In: CrystEngComm, Jg. 12 (2010-06-01), Heft 6, S. 1722-1725
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  7. Detailansicht für Treffer 7 öffnen
    Synthesis and crystal structure of two new heterometallic thioantimonates(III) [Ni(pda)2]CuI4SbIII2S6and [Ni(dien)2]CuISbIII3S6Electronic supplementary information (ESI) available: Selected distances and angles for 1and 2(Table S1); proposed hydrogen bonding geometry for 1and 2(Table S2). CCDC reference numbers 665818 for 1and 665819 for 2. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b906640c,Crystal data, for 1: Mw= 896.99. monoclinic, space group P2(1)/nwith a= 6.487(6), b= 15.345(15), c= 10.354(9), β= 90.617(10)°, V= 1030.6(17) Å3. T= 293(2) K, Z= 2, Dcalcd= 2.891g cm−3, µ= 8.128 mm−1. 7832 reflections collected in the range 2.3736 < < 27.4835, 2336 unique reflections. R1 = 0.0917 and wR2 = 0.1318 for 1521 observed reflections. For 2: Mw= 886.21. Monoclinic, space group P2(1)/cwith a= 17.107(4), b= 9.850(2), c= 14.530(3) , β= 103.559(4)°, V= 2380.2(9) Å3. T= 293(2) K, Z= 4, Dcalcd= 2.473g cm−3, µ= 5.551 mm−1. 17361 reflections collected in th
    Zhang, Meng ; Sheng, Tianlu ; et al.
    In: CrystEngComm, Jg. 12 (2010), Heft 1, S. 73-76
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  8. Detailansicht für Treffer 8 öffnen
    Structural similarities in Cs(16)-C86and C2(17)-C86Electronic supplementary information (ESI) available: Experimental procedure for isolation of Cs(16)-C86and C2(17)-C86, computational details, and crystallographic information, particularly details concerning the disorder. CCDC 771682. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c0cc00697a
    Wang, Zhimin ; Yang, Hua ; et al.
    In: Chemical Communications, Jg. 46 (2010-08-07), Heft 29, S. 5262-5264
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  9. Detailansicht für Treffer 9 öffnen
    Nonhydrolyzable analogs of phosphatidylinositol as ligands of phospholipases CThis article is part of a themed issue on Biophosphates.Electronic supplementary information (ESI) available: Characterization of lactone 23and ligand 10synthesis of intermediate 17. See DOI: 10.1039/b9nj00629j
    Mihai, Cornelia ; Yue, Xiangjun ; et al.
    In: New Journal of Chemistry, Jg. 34 (2010-05-01), Heft 5, S. 925-933
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  11. Detailansicht für Treffer 11 öffnen
    Stabilization of unusual discrete diorganotin carboxylates using the intramolecular coordination approach: synthesis, structure, TD-DFT, and Hirshfeld surface analyses.
    Mishra, Abhishek ; Chaudhary, Simran ; et al.
    In: New Journal of Chemistry, Jg. 47 (2023-09-28), Heft 36, S. 17129-17141
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  12. Detailansicht für Treffer 12 öffnen
    pH-Controlled change of the coordination modes of the highly symmetrical multitopic ligand and metal–oxygen arrays for constructing coordination assembliesElectronic supplementary information (ESI) available :  Detailed experimental procedures, structural description, PXRD patterns, and TGA of 1–4. CCDC reference numbers 732255 and 732257 for complexes 2–4. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/b917258kCrystal data for 1: C4H4O6Cd, Mr= 260.47, rhombohedral, space group R-3, a= 11.7673(9), b= 11.7673(9), c= 14.9293(16) , α= 90, β= 90, γ= 120°, V= 1790.3(3) Å3, Z= 9, µ= 2.726 mm−1, Dc= 2.174 Mg m−3, F(000) = 1116, T= 291(2) K, 3051 reflections collected, 746 unique with Rint= 0.0776, R1 = 0.0270, wR2 = 0.0596 (I >2σ(I)) and GOF = 1.103. Crystal data for 2: C8H2O10Cd3, Mr= 595.33, monoclinic, space group C2/m, a= 13.2366(13), b= 7.1753(6), c= 12.7690(12) , α= 90, β= 117.344(2), γ= 90°, V= 1077.25(17) Å3, Z= 4, µ= 5.925 mm−1, Dc= 3.671 Mg m−3,
    Zheng, Bo ; Bai, Junfeng ; et al.
    In: CrystEngComm, Jg. 12 (2010), Heft 1, S. 49-51
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  13. Detailansicht für Treffer 13 öffnen
    Mixed-magnesium/zinc calix[4]arene complexes: structure, and ring opening polymerisation studies.
    Banks, Henry J. S. ; Frese, Josef W. A. ; et al.
    In: Chemical Communications, Jg. 60 (2024-01-11), Heft 3, S. 304-307
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  14. Detailansicht für Treffer 14 öffnen
    Two pairs of chiral Yb<superscript>III</superscript> enantiomers presenting distinct NIR luminescence and circularly polarized luminescence performances with giant differences in second-harmonic generation responses.
    Du, Xiaodi ; Zhang, Zhiqiang ; et al.
    In: Dalton Transactions: An International Journal of Inorganic Chemistry, Jg. 52 (2023-12-21), Heft 47, S. 17758-17766
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  15. Detailansicht für Treffer 15 öffnen
    Self-loading lithographically structured microcontainers: 3D patterned, mobile microwells.
    Leong, TG ; Randall, CL ; et al.
    In: Lab on a chip, Jg. 8 (2008-10-01), Heft 10, S. 1621-4
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  16. Detailansicht für Treffer 16 öffnen
    A seven-coordinate Mn(II) complex with a pyridine-based 15-membered macrocyclic ligand containing one acetate pendant arm: structure, stability and relaxation properties.
    Praηáková, Marie ; Ndiaye, Daouda ; et al.
    In: Dalton Transactions: An International Journal of Inorganic Chemistry, Jg. 52 (2023-06-21), Heft 23, S. 7936-7947
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  17. Detailansicht für Treffer 17 öffnen
    A crystal engineering weaving of half-spiral molecules by hydrogen bonding chains into tube structuresElectronic supplementary information (ESI) available: Experimental procedures and crystal structure for 1. CCDC reference number 768466. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c1ce05663hSingle crystal X-ray diffraction data were collected on a Rigaku VariMax + Saturn724. using Mo-Kα radiation [λ= 0.71075 Å]: 1) C20H24F6O6, M= 474.40, orthorhombic, P212121(no. 19), a= 5.3232(10), b= 15.896(3), c= 25.664(5) Å, V= 2171.6(7) Å3, T= 93(1) K, Z= 4, μ= 1.377 cm−1, 17 639 reflections measured, 2859 unique (Rint= 0.034), wR2= 0.0814.
    Kataoka, Keisuke ; Yanagi, Masato ; et al.
    In: CrystEngComm, Jg. 13 (2011-10-12), Heft 21, S. 6342-6344
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  18. Detailansicht für Treffer 18 öffnen
    A flexible MMOF exhibiting high selectivity for CO2over N2, CH4and other small gasesElectronic supplementary information (ESI) available: Materials synthesis and activation details, selected crystallographic information, powder X-ray diffraction patterns, isosteric heat data and TGA profiles. CCDC 777415. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c0cc02942dCrystal data of 1: C23H21N2O5Zn, FW= 470.79, monoclinic, C2/c: a= 26.4310(18), b= 6.6400(5), c= 24.9341(17), β= 108.461(1)°, V= 4150.7(5) Å3, Z= 8, Dc= 1.507 g cm−3, λ(Mo-Kα) = 0.71073 Å, μ= 1.222. Measurements were made on a SMART CCD area detector at 100(2) K with graphite-monochromated Mo-Kα radiation. A total of 23 638 reflections were collected (6358 unique, R(int) = 0.0607) between a of 1.72° to 30.53° (99.8% completeness). R1= 0.0530 (I> 2(I)), wR= 0.1271 (all data), and GOF = 1.003 (all data). Largest diff. Peak and hole 1.213 and −1.095 e Å−3(See ESI for details). Compound 1(or RPM4
    Zhang, Jingming ; Wu, Haohan ; et al.
    In: Chemical Communications, Jg. 46 (2010-12-28), Heft 48, S. 9152-9154
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  19. Detailansicht für Treffer 19 öffnen
    Guanidine-centred reactivity of CNN Pd(II) pincer complexes including carboxylate-assisted N–H activation and –CH<subscript>2</subscript>– → –C(O)– oxygenation.
    Sinha, Nitish Kumar ; Khan, Hilal Ahmad ; et al.
    In: New Journal of Chemistry, Jg. 48 (2024-04-07), Heft 13, S. 5710-5720
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  20. Detailansicht für Treffer 20 öffnen
    Intermetallic transfer of unsymmetrical borylene fragments: isolation of the second early-transition-metal terminal borylene complex and other rare species.
    Macha, Bret B. ; Dhara, Debabrata ; et al.
    In: Dalton Transactions: An International Journal of Inorganic Chemistry, Jg. 49 (2020-12-28), Heft 48, S. 17719-17724
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