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Self-Inclusion Complexes Derived from Cyclodextrins: Synthesis and Characterization of 6(A),6(B)-Bis-O-[p-(allyloxy)phenyl]-Substituted beta-Cyclodextrins.

The Journal of organic chemistry

Chen Z, Bradshaw JS, Yi G, Pyo D, Black DR, Zimmerman SS, Lee ML, Tong W, D'Souza VT.
PMID: 11667876
J Org Chem. 1996 Dec 13;61(25):8949-8955. doi: 10.1021/jo960679i.

The syntheses, structures, and spectroscopic properties of 6(A),6(B)-bis-O-[p-(allyloxy)phenyl]-substituted beta-cyclodextrins have been investigated. Selective activation of the 6(A),6(B)-hydroxy groups was carried out by treating heptakis(2,3-di-O-methyl)-beta-cyclodextrin (1) with 2,4-dimethoxybenzene-1,5-disulfonyl chloride to give 6(A),6(B)-bissulfonate ester 2 in a yield of only 3%....

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Chen Z, Bradshaw JS, Yi G, et al. Self-Inclusion Complexes Derived from Cyclodextrins: Synthesis and Characterization of 6(A),6(B)-Bis-O-[p-(allyloxy)phenyl]-Substituted beta-Cyclodextrins. J Org Chem. 1996;61(25):8949-8955doi: 10.1021/jo960679i.
Chen, Z., Bradshaw, J. S., Yi, G., Pyo, D., Black, D. R., Zimmerman, S. S., Lee, M. L., Tong, W., & D'Souza, V. T. (1996). Self-Inclusion Complexes Derived from Cyclodextrins: Synthesis and Characterization of 6(A),6(B)-Bis-O-[p-(allyloxy)phenyl]-Substituted beta-Cyclodextrins. The Journal of organic chemistry, 61(25), 8949-8955. https://doi.org/10.1021/jo960679i
Chen, Zhen, et al. "Self-Inclusion Complexes Derived from Cyclodextrins: Synthesis and Characterization of 6(A),6(B)-Bis-O-[p-(allyloxy)phenyl]-Substituted beta-Cyclodextrins." The Journal of organic chemistry vol. 61,25 (1996): 8949-8955. doi: https://doi.org/10.1021/jo960679i
Chen Z, Bradshaw JS, Yi G, Pyo D, Black DR, Zimmerman SS, Lee ML, Tong W, D'Souza VT. Self-Inclusion Complexes Derived from Cyclodextrins: Synthesis and Characterization of 6(A),6(B)-Bis-O-[p-(allyloxy)phenyl]-Substituted beta-Cyclodextrins. J Org Chem. 1996 Dec 13;61(25):8949-8955. doi: 10.1021/jo960679i. PMID: 11667876.
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Compartmental Schiff-base ligands as selective double-loaded extractants for copper(II).

Chemical communications (Cambridge, England)

Black D, Blake AJ, Finn RL, Lindoy LF, Nezhadali A, Rougnaghi G, Tasker PA, Schröder M.
PMID: 12120064
Chem Commun (Camb). 2002 Feb 21;(4):340-1. doi: 10.1039/b109635b.

The Robson compartmental macrocyclic ligand derived from the condensation of derivatives of 2,6-diformylphenol and diamines has been prepared for the first time in its free ligand form; competitive three-phase transport and two-phase extraction studies confirm high double-loaded selectivity for...

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Black D, Blake AJ, Finn RL, et al. Compartmental Schiff-base ligands as selective double-loaded extractants for copper(II). Chem Commun (Camb). 2002;(4):340-1doi: 10.1039/b109635b.
Black, D., Blake, A. J., Finn, R. L., Lindoy, L. F., Nezhadali, A., Rougnaghi, G., Tasker, P. A., & Schröder, M. (2002). Compartmental Schiff-base ligands as selective double-loaded extractants for copper(II). Chemical communications (Cambridge, England), (4), 340-1. https://doi.org/10.1039/b109635b
Black, Daniel, et al. "Compartmental Schiff-base ligands as selective double-loaded extractants for copper(II)." Chemical communications (Cambridge, England) vol. ,4 (2002): 340-1. doi: https://doi.org/10.1039/b109635b
Black D, Blake AJ, Finn RL, Lindoy LF, Nezhadali A, Rougnaghi G, Tasker PA, Schröder M. Compartmental Schiff-base ligands as selective double-loaded extractants for copper(II). Chem Commun (Camb). 2002 Feb 21;(4):340-1. doi: 10.1039/b109635b. PMID: 12120064.
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Azatriquinanes: Synthesis, Structure, and Reactivity.

The Journal of organic chemistry

Hext NM, Hansen J, Blake AJ, Hibbs DE, Hursthouse MB, Shishkin OV, Mascal M.
PMID: 11672206
J Org Chem. 1998 Aug 21;63(17):6016-6020. doi: 10.1021/jo980788s.

Azatriquinane, a tricyclic amine with rigid, hemispherical topology, is synthesized in six steps from pyrrole. This first example of a [2.2.2]cyclazine can be oxidatively dimerized to a novel, highly strained heptacycle or oxidized with chlorine to give an azatriquinacene,...

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Hext NM, Hansen J, Blake AJ, et al. Azatriquinanes: Synthesis, Structure, and Reactivity. J Org Chem. 1998;63(17):6016-6020doi: 10.1021/jo980788s.
Hext, N. M., Hansen, J., Blake, A. J., Hibbs, D. E., Hursthouse, M. B., Shishkin, O. V., & Mascal, M. (1998). Azatriquinanes: Synthesis, Structure, and Reactivity. The Journal of organic chemistry, 63(17), 6016-6020. https://doi.org/10.1021/jo980788s
Hext, Nicholas M., et al. "Azatriquinanes: Synthesis, Structure, and Reactivity." The Journal of organic chemistry vol. 63,17 (1998): 6016-6020. doi: https://doi.org/10.1021/jo980788s
Hext NM, Hansen J, Blake AJ, Hibbs DE, Hursthouse MB, Shishkin OV, Mascal M. Azatriquinanes: Synthesis, Structure, and Reactivity. J Org Chem. 1998 Aug 21;63(17):6016-6020. doi: 10.1021/jo980788s. PMID: 11672206.
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Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor.

Chemical communications (Cambridge, England)

Blake AJ, Brett MT, Champness NR, Khlobystov AN, Long DL, Wilson C, Schröder M.
PMID: 12240139
Chem Commun (Camb). 2001 Nov 07;(21):2258-9. doi: 10.1039/b106348k.

4,4'-Bipyridine N,N'-dioxide (L) acts as a hydrogen-bond acceptor in the compounds ([M(NO3)2(H2O)4].L2) (M = Co, Ni) to form doubly-interpenetrated framework materials with sixfold topological connectivity.

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Blake AJ, Brett MT, Champness NR, et al. Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor. Chem Commun (Camb). 2001;(21):2258-9doi: 10.1039/b106348k.
Blake, A. J., Brett, M. T., Champness, N. R., Khlobystov, A. N., Long, D. L., Wilson, C., & Schröder, M. (2001). Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor. Chemical communications (Cambridge, England), (21), 2258-9. https://doi.org/10.1039/b106348k
Blake, A J, et al. "Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor." Chemical communications (Cambridge, England) vol. ,21 (2001): 2258-9. doi: https://doi.org/10.1039/b106348k
Blake AJ, Brett MT, Champness NR, Khlobystov AN, Long DL, Wilson C, Schröder M. Inorganic-organic interpenetrating frameworks: 4,4'-bipyridine N,N'-dioxide as a bridging hydrogen-bond acceptor. Chem Commun (Camb). 2001 Nov 07;(21):2258-9. doi: 10.1039/b106348k. PMID: 12240139.
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Helical templating of polyiodide networks at a binuclear metallo complex.

Chemical communications (Cambridge, England)

Horn CJ, Blake AJ, Champness NR, Garau A, Lippolis V, Wilson C, Schröder M.
PMID: 12613588
Chem Commun (Camb). 2003 Feb 07;(3):312-3. doi: 10.1039/b211743f.

A homobimetallic supramolecular helicate has been prepared from a new multimodal ligand, and used to template the formation of two polyiodide networks, one containing an unprecedented figure-of-eight polyiodide helix, the other dominated by peripheral C-H...I polyiodide chain interactions.

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Horn CJ, Blake AJ, Champness NR, et al. Helical templating of polyiodide networks at a binuclear metallo complex. Chem Commun (Camb). 2003;(3):312-3doi: 10.1039/b211743f.
Horn, C. J., Blake, A. J., Champness, N. R., Garau, A., Lippolis, V., Wilson, C., & Schröder, M. (2003). Helical templating of polyiodide networks at a binuclear metallo complex. Chemical communications (Cambridge, England), (3), 312-3. https://doi.org/10.1039/b211743f
Horn, Caitlin J, et al. "Helical templating of polyiodide networks at a binuclear metallo complex." Chemical communications (Cambridge, England) vol. ,3 (2003): 312-3. doi: https://doi.org/10.1039/b211743f
Horn CJ, Blake AJ, Champness NR, Garau A, Lippolis V, Wilson C, Schröder M. Helical templating of polyiodide networks at a binuclear metallo complex. Chem Commun (Camb). 2003 Feb 07;(3):312-3. doi: 10.1039/b211743f. PMID: 12613588.
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Titanium and zirconium complexes supported by dipyrrolide ligands.

Chemical communications (Cambridge, England)

Novak A, Blake AJ, Wilson C, Love JB.
PMID: 12478751
Chem Commun (Camb). 2002 Dec 07;(23):2796-7. doi: 10.1039/b208751k.

The reactions between meso-disubstituted dipyrromethanes and titanium and zirconium amides and alkyls have generated the first examples of dipyrrolide complexes of Group 4 metals.

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Novak A, Blake AJ, Wilson C, et al. Titanium and zirconium complexes supported by dipyrrolide ligands. Chem Commun (Camb). 2002;(23):2796-7doi: 10.1039/b208751k.
Novak, A., Blake, A. J., Wilson, C., & Love, J. B. (2002). Titanium and zirconium complexes supported by dipyrrolide ligands. Chemical communications (Cambridge, England), (23), 2796-7. https://doi.org/10.1039/b208751k
Novak, Andrew, et al. "Titanium and zirconium complexes supported by dipyrrolide ligands." Chemical communications (Cambridge, England) vol. ,23 (2002): 2796-7. doi: https://doi.org/10.1039/b208751k
Novak A, Blake AJ, Wilson C, Love JB. Titanium and zirconium complexes supported by dipyrrolide ligands. Chem Commun (Camb). 2002 Dec 07;(23):2796-7. doi: 10.1039/b208751k. PMID: 12478751.
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Continuum percolation threshold for interpenetrating squares and cubes.

Physical review. E, Statistical, nonlinear, and soft matter physics

Baker DR, Paul G, Sreenivasan S, Stanley HE.
PMID: 12443288
Phys Rev E Stat Nonlin Soft Matter Phys. 2002 Oct;66(4):046136. doi: 10.1103/PhysRevE.66.046136. Epub 2002 Oct 30.

Monte Carlo simulations are performed to determine the critical percolation threshold for interpenetrating square objects in two dimensions and cubic objects in three dimensions. Simulations are performed for two cases: (i) objects whose edges are aligned parallel to one...

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Baker DR, Paul G, Sreenivasan S, et al. Continuum percolation threshold for interpenetrating squares and cubes. Phys Rev E Stat Nonlin Soft Matter Phys. 2002;66(4):046136doi: 10.1103/PhysRevE.66.046136.
Baker, D. R., Paul, G., Sreenivasan, S., & Stanley, H. E. (2002). Continuum percolation threshold for interpenetrating squares and cubes. Physical review. E, Statistical, nonlinear, and soft matter physics, 66(4), 046136. https://doi.org/10.1103/PhysRevE.66.046136
Baker, Don R, et al. "Continuum percolation threshold for interpenetrating squares and cubes." Physical review. E, Statistical, nonlinear, and soft matter physics vol. 66,4 (2002): 046136. doi: https://doi.org/10.1103/PhysRevE.66.046136
Baker DR, Paul G, Sreenivasan S, Stanley HE. Continuum percolation threshold for interpenetrating squares and cubes. Phys Rev E Stat Nonlin Soft Matter Phys. 2002 Oct;66(4):046136. doi: 10.1103/PhysRevE.66.046136. Epub 2002 Oct 30. PMID: 12443288.
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Unprecedented Seven- and Eight-Connected Lanthanide Coordination Networks This work was supported by the Royal Society and the Engineering and Physical Sciences Research Council (Royal Society K. C. Wong and EPSRC postdoctoral fellowships to D.-L.L.). .

Angewandte Chemie (International ed. in English)

Long DL, Blake AJ, Champness NR, Wilson C, Schröder M.
PMID: 11443659
Angew Chem Int Ed Engl. 2001 Jul 02;40(13):2443-2447.

No abstract available.

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Long DL, Blake AJ, Champness NR, et al. Unprecedented Seven- and Eight-Connected Lanthanide Coordination Networks This work was supported by the Royal Society and the Engineering and Physical Sciences Research Council (Royal Society K. C. Wong and EPSRC postdoctoral fellowships to D.-L.L.). . Angew Chem Int Ed Engl. 2001;40(13):2443-2447
Long, D. L., Blake, A. J., Champness, N. R., Wilson, C., & Schröder, M. (2001). Unprecedented Seven- and Eight-Connected Lanthanide Coordination Networks This work was supported by the Royal Society and the Engineering and Physical Sciences Research Council (Royal Society K. C. Wong and EPSRC postdoctoral fellowships to D.-L.L.). . Angewandte Chemie (International ed. in English), 40(13), 2443-2447.
Long, De-Liang, et al. "Unprecedented Seven- and Eight-Connected Lanthanide Coordination Networks This work was supported by the Royal Society and the Engineering and Physical Sciences Research Council (Royal Society K. C. Wong and EPSRC postdoctoral fellowships to D.-L.L.). ." Angewandte Chemie (International ed. in English) vol. 40,13 (2001): 2443-2447.
Long DL, Blake AJ, Champness NR, Wilson C, Schröder M. Unprecedented Seven- and Eight-Connected Lanthanide Coordination Networks This work was supported by the Royal Society and the Engineering and Physical Sciences Research Council (Royal Society K. C. Wong and EPSRC postdoctoral fellowships to D.-L.L.). . Angew Chem Int Ed Engl. 2001 Jul 02;40(13):2443-2447. PMID: 11443659.
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Evidence from the Pacific troposphere for large global sources of oxygenated organic compounds.

Nature

Singh H, Chen Y, Staudt A, Jacob D, Blake D, Heikes B, Snow J.
PMID: 11323667
Nature. 2001 Apr 26;410(6832):1078-81. doi: 10.1038/35074067.

The presence of oxygenated organic compounds in the troposphere strongly influences key atmospheric processes. Such oxygenated species are, for example, carriers of reactive nitrogen and are easily photolysed, producing free radicals-and so influence the oxidizing capacity and the ozone-forming...

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Singh H, Chen Y, Staudt A, et al. Evidence from the Pacific troposphere for large global sources of oxygenated organic compounds. Nature. 2001;410(6832):1078-81doi: 10.1038/35074067.
Singh, H., Chen, Y., Staudt, A., Jacob, D., Blake, D., Heikes, B., & Snow, J. (2001). Evidence from the Pacific troposphere for large global sources of oxygenated organic compounds. Nature, 410(6832), 1078-81. https://doi.org/10.1038/35074067
Singh, H, et al. "Evidence from the Pacific troposphere for large global sources of oxygenated organic compounds." Nature vol. 410,6832 (2001): 1078-81. doi: https://doi.org/10.1038/35074067
Singh H, Chen Y, Staudt A, Jacob D, Blake D, Heikes B, Snow J. Evidence from the Pacific troposphere for large global sources of oxygenated organic compounds. Nature. 2001 Apr 26;410(6832):1078-81. doi: 10.1038/35074067. PMID: 11323667.
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Dynamic equilibria in the products of intramolecular Buchner additions of diazoketones to aryl rings bearing methoxy substituents.

The Journal of organic chemistry

Maguire AR, O'Leary P, Harrington F, Lawrence SE, Blake AJ.
PMID: 11597247
J Org Chem. 2001 Oct 19;66(21):7166-77. doi: 10.1021/jo015750l.

Rhodium carboxylate catalyzed aromatic addition reactions of a range of diazoketones bearing methoxy-substituted aryl rings have been explored. While the existence of norcaradiene-cycloheptatriene equilibria in related compounds is well established, the aromatic addition products in this study display more...

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Maguire AR, O'Leary P, Harrington F, et al. Dynamic equilibria in the products of intramolecular Buchner additions of diazoketones to aryl rings bearing methoxy substituents. J Org Chem. 2001;66(21):7166-77doi: 10.1021/jo015750l.
Maguire, A. R., O'Leary, P., Harrington, F., Lawrence, S. E., & Blake, A. J. (2001). Dynamic equilibria in the products of intramolecular Buchner additions of diazoketones to aryl rings bearing methoxy substituents. The Journal of organic chemistry, 66(21), 7166-77. https://doi.org/10.1021/jo015750l
Maguire, A R, et al. "Dynamic equilibria in the products of intramolecular Buchner additions of diazoketones to aryl rings bearing methoxy substituents." The Journal of organic chemistry vol. 66,21 (2001): 7166-77. doi: https://doi.org/10.1021/jo015750l
Maguire AR, O'Leary P, Harrington F, Lawrence SE, Blake AJ. Dynamic equilibria in the products of intramolecular Buchner additions of diazoketones to aryl rings bearing methoxy substituents. J Org Chem. 2001 Oct 19;66(21):7166-77. doi: 10.1021/jo015750l. PMID: 11597247.
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Non-natural eight-connected solid-state materials: a new coordination chemistry.

Angewandte Chemie (International ed. in English)

Long DL, Hill RJ, Blake AJ, Champness NR, Hubberstey P, Proserpio DM, Wilson C, Schröder M.
PMID: 15054793
Angew Chem Int Ed Engl. 2004 Mar 26;43(14):1851-4. doi: 10.1002/anie.200352625.

No abstract available.

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Long DL, Hill RJ, Blake AJ, et al. Non-natural eight-connected solid-state materials: a new coordination chemistry. Angew Chem Int Ed Engl. 2004;43(14):1851-4doi: 10.1002/anie.200352625.
Long, D. L., Hill, R. J., Blake, A. J., Champness, N. R., Hubberstey, P., Proserpio, D. M., Wilson, C., & Schröder, M. (2004). Non-natural eight-connected solid-state materials: a new coordination chemistry. Angewandte Chemie (International ed. in English), 43(14), 1851-4. https://doi.org/10.1002/anie.200352625
Long, De-Liang, et al. "Non-natural eight-connected solid-state materials: a new coordination chemistry." Angewandte Chemie (International ed. in English) vol. 43,14 (2004): 1851-4. doi: https://doi.org/10.1002/anie.200352625
Long DL, Hill RJ, Blake AJ, Champness NR, Hubberstey P, Proserpio DM, Wilson C, Schröder M. Non-natural eight-connected solid-state materials: a new coordination chemistry. Angew Chem Int Ed Engl. 2004 Mar 26;43(14):1851-4. doi: 10.1002/anie.200352625. PMID: 15054793.
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PtII diimine chromophores with perfluorinated thiolate ligands: nature and dynamics of the charge-transfer-to-diimine lowest excited state.

Inorganic chemistry

Weinstein JA, Blake AJ, Davies ES, Davis AL, George MW, Grills DC, Lileev IV, Maksimov AM, Matousek P, Mel'nikov MY, Parker AW, Platonov VE, Towrie M, Wilson C, Zheligovskaya NN.
PMID: 14577775
Inorg Chem. 2003 Nov 03;42(22):7077-85. doi: 10.1021/ic026286l.

The synthesis of new Pt(II) diimine complexes bearing perfluorinated thiolate ligands, Pt(II)(NN)(4-X-C(6)F(4)-S)(2), where NN = 2,2'-bipyridine or 1,10-phenanthroline and X = F or CN, is reported, together with an investigation of the nature and dynamics of their lowest excited...

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Weinstein JA, Blake AJ, Davies ES, et al. PtII diimine chromophores with perfluorinated thiolate ligands: nature and dynamics of the charge-transfer-to-diimine lowest excited state. Inorg Chem. 2003;42(22):7077-85doi: 10.1021/ic026286l.
Weinstein, J. A., Blake, A. J., Davies, E. S., Davis, A. L., George, M. W., Grills, D. C., Lileev, I. V., Maksimov, A. M., Matousek, P., Mel'nikov, M. Y., Parker, A. W., Platonov, V. E., Towrie, M., Wilson, C., & Zheligovskaya, N. N. (2003). PtII diimine chromophores with perfluorinated thiolate ligands: nature and dynamics of the charge-transfer-to-diimine lowest excited state. Inorganic chemistry, 42(22), 7077-85. https://doi.org/10.1021/ic026286l
Weinstein, Julia A, et al. "PtII diimine chromophores with perfluorinated thiolate ligands: nature and dynamics of the charge-transfer-to-diimine lowest excited state." Inorganic chemistry vol. 42,22 (2003): 7077-85. doi: https://doi.org/10.1021/ic026286l
Weinstein JA, Blake AJ, Davies ES, Davis AL, George MW, Grills DC, Lileev IV, Maksimov AM, Matousek P, Mel'nikov MY, Parker AW, Platonov VE, Towrie M, Wilson C, Zheligovskaya NN. PtII diimine chromophores with perfluorinated thiolate ligands: nature and dynamics of the charge-transfer-to-diimine lowest excited state. Inorg Chem. 2003 Nov 03;42(22):7077-85. doi: 10.1021/ic026286l. PMID: 14577775.
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Showing 25 to 36 of 684 entries