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Polynuclear lanthanide (Ln) complexes of a tri-functional hydrazone ligand--mononuclear (Dy), dinuclear (Yb, Tm), tetranuclear (Gd), and hexanuclear (Gd, Dy, Tb) examples.

Dalton transactions (Cambridge, England : 2003)

Anwar MU, Dawe LN, Tandon SS, Bunge SD, Thompson LK.
PMID: 23552191
Dalton Trans. 2013 Jun 07;42(21):7781-94. doi: 10.1039/c3dt32732a.

The lanthanide coordination chemistry of a tri-functional vanillin-hydrazone-oxime ligand reveals a variety of different products, depending on reaction conditions, with mono-nuclear (Dy), dinuclear (Yb, Tm), tetranuclear (Gd) and hexanuclear (Gd, Tb, Dy) examples. The Ln6 (Ln = Gd, Dy,...

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Anwar MU, Dawe LN, Tandon SS, et al. Polynuclear lanthanide (Ln) complexes of a tri-functional hydrazone ligand--mononuclear (Dy), dinuclear (Yb, Tm), tetranuclear (Gd), and hexanuclear (Gd, Dy, Tb) examples. Dalton Trans. 2013;42(21):7781-94doi: 10.1039/c3dt32732a.
Anwar, M. U., Dawe, L. N., Tandon, S. S., Bunge, S. D., & Thompson, L. K. (2013). Polynuclear lanthanide (Ln) complexes of a tri-functional hydrazone ligand--mononuclear (Dy), dinuclear (Yb, Tm), tetranuclear (Gd), and hexanuclear (Gd, Dy, Tb) examples. Dalton transactions (Cambridge, England : 2003), 42(21), 7781-94. https://doi.org/10.1039/c3dt32732a
Anwar, Muhammad U, et al. "Polynuclear lanthanide (Ln) complexes of a tri-functional hydrazone ligand--mononuclear (Dy), dinuclear (Yb, Tm), tetranuclear (Gd), and hexanuclear (Gd, Dy, Tb) examples." Dalton transactions (Cambridge, England : 2003) vol. 42,21 (2013): 7781-94. doi: https://doi.org/10.1039/c3dt32732a
Anwar MU, Dawe LN, Tandon SS, Bunge SD, Thompson LK. Polynuclear lanthanide (Ln) complexes of a tri-functional hydrazone ligand--mononuclear (Dy), dinuclear (Yb, Tm), tetranuclear (Gd), and hexanuclear (Gd, Dy, Tb) examples. Dalton Trans. 2013 Jun 07;42(21):7781-94. doi: 10.1039/c3dt32732a. PMID: 23552191.
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Ring-opening polymerization of rac-lactide mediated by tetrametallic lithium and sodium diamino-bis(phenolate) complexes.

Dalton transactions (Cambridge, England : 2003)

Alhashmialameer D, Ikpo N, Collins J, Dawe LN, Hattenhauer K, Kerton FM.
PMID: 26538475
Dalton Trans. 2015 Dec 14;44(46):20216-31. doi: 10.1039/c5dt03119b.

Lithium and sodium compounds supported by tetradentate amino-bis(phenolato) ligands, [Li2(N2O2(BuBuPip))] (1), [Na2(N2O2(BuBuPip))] (2) (where [N2O2(BuBuPip)] = 2,2'-N,N'-homopiperazinyl-bis(2-methylene-4,6-tert-butylphenol), and [Li2(N2O2(BuMePip))] (3), [Na2(N2O2(BuMePip))] (4) (where [N2O2(BuMePip)] = 2,2'-N,N'-homopiperazinyl-bis(2-methylene-4-methyl-6-tert-butylphenol) were synthesized and characterized by NMR spectroscopy and MALDI-TOF mass spectrometry. Variable temperature...

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Alhashmialameer D, Ikpo N, Collins J, et al. Ring-opening polymerization of rac-lactide mediated by tetrametallic lithium and sodium diamino-bis(phenolate) complexes. Dalton Trans. 2015;44(46):20216-31doi: 10.1039/c5dt03119b.
Alhashmialameer, D., Ikpo, N., Collins, J., Dawe, L. N., Hattenhauer, K., & Kerton, F. M. (2015). Ring-opening polymerization of rac-lactide mediated by tetrametallic lithium and sodium diamino-bis(phenolate) complexes. Dalton transactions (Cambridge, England : 2003), 44(46), 20216-31. https://doi.org/10.1039/c5dt03119b
Alhashmialameer, Dalal, et al. "Ring-opening polymerization of rac-lactide mediated by tetrametallic lithium and sodium diamino-bis(phenolate) complexes." Dalton transactions (Cambridge, England : 2003) vol. 44,46 (2015): 20216-31. doi: https://doi.org/10.1039/c5dt03119b
Alhashmialameer D, Ikpo N, Collins J, Dawe LN, Hattenhauer K, Kerton FM. Ring-opening polymerization of rac-lactide mediated by tetrametallic lithium and sodium diamino-bis(phenolate) complexes. Dalton Trans. 2015 Dec 14;44(46):20216-31. doi: 10.1039/c5dt03119b. PMID: 26538475.
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Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not.

The Journal of organic chemistry

Boger DL, Garbaccio RM.
PMID: 11674637
J Org Chem. 1999 Jul 23;64(15):5666-5669. doi: 10.1021/jo990762g.

A study of the solvolysis pH-rate profiles for two key reactive CC-1065/duocarmycin alkylation subunit analogues is detailed. Unlike the authentic alkylation subunits and N-BOC-CBI (4) which are too stable to establish complete solvolysis pH-rate profiles, the analogues N-BOC-CBQ (5)...

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Boger DL, Garbaccio RM. Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not. J Org Chem. 1999;64(15):5666-5669doi: 10.1021/jo990762g.
Boger, D. L., & Garbaccio, R. M. (1999). Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not. The Journal of organic chemistry, 64(15), 5666-5669. https://doi.org/10.1021/jo990762g
Boger, Dale L., and Garbaccio, Robert M.. "Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not." The Journal of organic chemistry vol. 64,15 (1999): 5666-5669. doi: https://doi.org/10.1021/jo990762g
Boger DL, Garbaccio RM. Are the Duocarmycin and CC-1065 DNA Alkylation Reactions Acid-Catalyzed? Solvolysis pH-Rate Profiles Suggest They Are Not. J Org Chem. 1999 Jul 23;64(15):5666-5669. doi: 10.1021/jo990762g. PMID: 11674637.
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CC-1065 and the Duocarmycins: Synthetic Studies.

Chemical reviews

Boger DL, Boyce CW, Garbaccio RM, Goldberg JA.
PMID: 11848889
Chem Rev. 1997 May 08;97(3):787-828. doi: 10.1021/cr960095g.

No abstract available.

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Boger DL, Boyce CW, Garbaccio RM, et al. CC-1065 and the Duocarmycins: Synthetic Studies. Chem Rev. 1997;97(3):787-828doi: 10.1021/cr960095g.
Boger, D. L., Boyce, C. W., Garbaccio, R. M., & Goldberg, J. A. (1997). CC-1065 and the Duocarmycins: Synthetic Studies. Chemical reviews, 97(3), 787-828. https://doi.org/10.1021/cr960095g
Boger, Dale L., et al. "CC-1065 and the Duocarmycins: Synthetic Studies." Chemical reviews vol. 97,3 (1997): 787-828. doi: https://doi.org/10.1021/cr960095g
Boger DL, Boyce CW, Garbaccio RM, Goldberg JA. CC-1065 and the Duocarmycins: Synthetic Studies. Chem Rev. 1997 May 08;97(3):787-828. doi: 10.1021/cr960095g. PMID: 11848889.
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Comparative diversity and composition of cyanobacteria in three predominant soil crusts of the Colorado Plateau.

FEMS microbiology ecology

Redfield E, Barns SM, Belnap J, Daane LL, Kuske CR.
PMID: 19709211
FEMS Microbiol Ecol. 2002 Apr 01;40(1):55-63. doi: 10.1111/j.1574-6941.2002.tb00936.x.

Terminal restriction fragment length polymorphism (TRF or T-RFLP) analysis and 16S rDNA sequence analysis from clone libraries were used to examine cyanobacterial diversity in three types of predominant soil crusts in an arid grassland. Total DNA was extracted from...

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Redfield E, Barns SM, Belnap J, et al. Comparative diversity and composition of cyanobacteria in three predominant soil crusts of the Colorado Plateau. FEMS Microbiol Ecol. 2002;40(1):55-63doi: 10.1111/j.1574-6941.2002.tb00936.x.
Redfield, E., Barns, S. M., Belnap, J., Daane, L. L., & Kuske, C. R. (2002). Comparative diversity and composition of cyanobacteria in three predominant soil crusts of the Colorado Plateau. FEMS microbiology ecology, 40(1), 55-63. https://doi.org/10.1111/j.1574-6941.2002.tb00936.x
Redfield, Elizabeth, et al. "Comparative diversity and composition of cyanobacteria in three predominant soil crusts of the Colorado Plateau." FEMS microbiology ecology vol. 40,1 (2002): 55-63. doi: https://doi.org/10.1111/j.1574-6941.2002.tb00936.x
Redfield E, Barns SM, Belnap J, Daane LL, Kuske CR. Comparative diversity and composition of cyanobacteria in three predominant soil crusts of the Colorado Plateau. FEMS Microbiol Ecol. 2002 Apr 01;40(1):55-63. doi: 10.1111/j.1574-6941.2002.tb00936.x. PMID: 19709211.
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A self-assembled, magnetically coupled square Cu16 4x[2x2] grid.

Angewandte Chemie (International ed. in English)

Dawe LN, Thompson LK.
PMID: 17702078
Angew Chem Int Ed Engl. 2007;46(39):7440-4. doi: 10.1002/anie.200701840.

No abstract available.

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Dawe LN, Thompson LK. A self-assembled, magnetically coupled square Cu16 4x[2x2] grid. Angew Chem Int Ed Engl. 2007;46(39):7440-4doi: 10.1002/anie.200701840.
Dawe, L. N., & Thompson, L. K. (2007). A self-assembled, magnetically coupled square Cu16 4x[2x2] grid. Angewandte Chemie (International ed. in English), 46(39), 7440-4. https://doi.org/10.1002/anie.200701840
Dawe, Louise N, and Thompson, Laurence K. "A self-assembled, magnetically coupled square Cu16 4x[2x2] grid." Angewandte Chemie (International ed. in English) vol. 46,39 (2007): 7440-4. doi: https://doi.org/10.1002/anie.200701840
Dawe LN, Thompson LK. A self-assembled, magnetically coupled square Cu16 4x[2x2] grid. Angew Chem Int Ed Engl. 2007;46(39):7440-4. doi: 10.1002/anie.200701840. PMID: 17702078.
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Ligand directed self-assembly of polymetallic [n x n] grids: rational routes to large functional molecular subunits?.

Dalton transactions (Cambridge, England : 2003)

Dawe LN, Abedin TS, Thompson LK.
PMID: 18354761
Dalton Trans. 2008 Apr 07;(13):1661-75. doi: 10.1039/b716114j. Epub 2007 Dec 17.

Poly-(n)-topic ligands with a linear arrangement of coordination pockets self-assemble, generally in high yield, to produce square [n x n] grid complexes. Oligomeric, non-grid intermediates, identified by structural studies, have shown alternative construction pathways, but have also indicated possible...

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Dawe LN, Abedin TS, Thompson LK. Ligand directed self-assembly of polymetallic [n x n] grids: rational routes to large functional molecular subunits?. Dalton Trans. 2007;(13):1661-75doi: 10.1039/b716114j.
Dawe, L. N., Abedin, T. S., & Thompson, L. K. (2008). Ligand directed self-assembly of polymetallic [n x n] grids: rational routes to large functional molecular subunits?. Dalton transactions (Cambridge, England : 2003), (13), 1661-75. https://doi.org/10.1039/b716114j
Dawe, Louise N, et al. "Ligand directed self-assembly of polymetallic [n x n] grids: rational routes to large functional molecular subunits?." Dalton transactions (Cambridge, England : 2003) vol. ,13 (2008): 1661-75. doi: https://doi.org/10.1039/b716114j
Dawe LN, Abedin TS, Thompson LK. Ligand directed self-assembly of polymetallic [n x n] grids: rational routes to large functional molecular subunits?. Dalton Trans. 2008 Apr 07;(13):1661-75. doi: 10.1039/b716114j. Epub 2007 Dec 17. PMID: 18354761.
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Supramolecular 'flat' Mn9 grid complexes--towards functional molecular platforms.

Dalton transactions (Cambridge, England : 2003)

Milway VA, Abedin SM, Niel V, Kelly TL, Dawe LN, Dey SK, Thompson DW, Miller DO, Alam MS, Müller P, Thompson LK.
PMID: 16751892
Dalton Trans. 2006 Jun 21;(23):2835-51. doi: 10.1039/b515801j. Epub 2006 May 12.

Flat, quantum dot like arrays of closely spaced, electron rich metal centres are seen as attractive subunits for device capability at the molecular level. Mn(II)9 grids, formed by self-assembly processes using 'tritopic' pyridine-2,6-dihydrazone ligands, provide easy and pre-programmable routes...

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Milway VA, Abedin SM, Niel V, et al. Supramolecular 'flat' Mn9 grid complexes--towards functional molecular platforms. Dalton Trans. 2006;(23):2835-51doi: 10.1039/b515801j.
Milway, V. A., Abedin, S. M., Niel, V., Kelly, T. L., Dawe, L. N., Dey, S. K., Thompson, D. W., Miller, D. O., Alam, M. S., Müller, P., & Thompson, L. K. (2006). Supramolecular 'flat' Mn9 grid complexes--towards functional molecular platforms. Dalton transactions (Cambridge, England : 2003), (23), 2835-51. https://doi.org/10.1039/b515801j
Milway, Victoria A, et al. "Supramolecular 'flat' Mn9 grid complexes--towards functional molecular platforms." Dalton transactions (Cambridge, England : 2003) vol. ,23 (2006): 2835-51. doi: https://doi.org/10.1039/b515801j
Milway VA, Abedin SM, Niel V, Kelly TL, Dawe LN, Dey SK, Thompson DW, Miller DO, Alam MS, Müller P, Thompson LK. Supramolecular 'flat' Mn9 grid complexes--towards functional molecular platforms. Dalton Trans. 2006 Jun 21;(23):2835-51. doi: 10.1039/b515801j. Epub 2006 May 12. PMID: 16751892.
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Coordination "oligomers" in self-assembly reactions of some "tritopic" picolinic dihydrazone ligands-mononuclear, dinuclear, hexanuclear, heptanuclear, and nonanuclear examples.

Inorganic chemistry

Niel V, Milway VA, Dawe LN, Grove H, Tandon SS, Abedin TS, Kelly TL, Spencer EC, Howard JA, Collins JL, Miller DO, Thompson LK.
PMID: 18076158
Inorg Chem. 2008 Jan 07;47(1):176-89. doi: 10.1021/ic7016787. Epub 2007 Dec 13.

"Tritopic" picolinic dihydrazone ligands with tridentate coordination pockets are designed to produce homoleptic [3 x 3] nonanuclear square grid complexes on reaction with transition-metal salts, and many structurally documented examples have been obtained with Mn(II), Cu(II), and Zn(II) ions....

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Niel V, Milway VA, Dawe LN, et al. Coordination "oligomers" in self-assembly reactions of some "tritopic" picolinic dihydrazone ligands-mononuclear, dinuclear, hexanuclear, heptanuclear, and nonanuclear examples. Inorg Chem. 2007;47(1):176-89doi: 10.1021/ic7016787.
Niel, V., Milway, V. A., Dawe, L. N., Grove, H., Tandon, S. S., Abedin, T. S., Kelly, T. L., Spencer, E. C., Howard, J. A., Collins, J. L., Miller, D. O., & Thompson, L. K. (2008). Coordination "oligomers" in self-assembly reactions of some "tritopic" picolinic dihydrazone ligands-mononuclear, dinuclear, hexanuclear, heptanuclear, and nonanuclear examples. Inorganic chemistry, 47(1), 176-89. https://doi.org/10.1021/ic7016787
Niel, Virginie, et al. "Coordination "oligomers" in self-assembly reactions of some "tritopic" picolinic dihydrazone ligands-mononuclear, dinuclear, hexanuclear, heptanuclear, and nonanuclear examples." Inorganic chemistry vol. 47,1 (2008): 176-89. doi: https://doi.org/10.1021/ic7016787
Niel V, Milway VA, Dawe LN, Grove H, Tandon SS, Abedin TS, Kelly TL, Spencer EC, Howard JA, Collins JL, Miller DO, Thompson LK. Coordination "oligomers" in self-assembly reactions of some "tritopic" picolinic dihydrazone ligands-mononuclear, dinuclear, hexanuclear, heptanuclear, and nonanuclear examples. Inorg Chem. 2008 Jan 07;47(1):176-89. doi: 10.1021/ic7016787. Epub 2007 Dec 13. PMID: 18076158.
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Synthesis and clathrates of oligomeric 2-O-naphthoide macrocycles.

The Journal of organic chemistry

AlHujran TA, Dawe LN, Collins J, Georghiou PE.
PMID: 21229978
J Org Chem. 2011 Feb 04;76(3):971-3. doi: 10.1021/jo101959w. Epub 2011 Jan 13.

New macrocyclic O-naphthoides 4-6 were synthesized from dehydration reactions of 3-hydroxy- and 7-tert-butyl-3-hydroxy-2-naphthoic acids, respectively. Their X-ray structures were determined and their clathrate inclusion properties were investigated. Hexamer 6 formed an inclusion clathrate with four chloroform molecules. The trimer...

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AlHujran TA, Dawe LN, Collins J, et al. Synthesis and clathrates of oligomeric 2-O-naphthoide macrocycles. J Org Chem. 2011;76(3):971-3doi: 10.1021/jo101959w.
AlHujran, T. A., Dawe, L. N., Collins, J., & Georghiou, P. E. (2011). Synthesis and clathrates of oligomeric 2-O-naphthoide macrocycles. The Journal of organic chemistry, 76(3), 971-3. https://doi.org/10.1021/jo101959w
AlHujran, Tayel A, et al. "Synthesis and clathrates of oligomeric 2-O-naphthoide macrocycles." The Journal of organic chemistry vol. 76,3 (2011): 971-3. doi: https://doi.org/10.1021/jo101959w
AlHujran TA, Dawe LN, Collins J, Georghiou PE. Synthesis and clathrates of oligomeric 2-O-naphthoide macrocycles. J Org Chem. 2011 Feb 04;76(3):971-3. doi: 10.1021/jo101959w. Epub 2011 Jan 13. PMID: 21229978.
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Supramolecular self-assembled polynuclear complexes from tritopic, tetratopic, and pentatopic ligands: structural, magnetic and surface studies.

Inorganic chemistry

Dey SK, Abedin TS, Dawe LN, Tandon SS, Collins JL, Thompson LK, Postnikov AV, Alam MS, Müller P.
PMID: 17696336
Inorg Chem. 2007 Sep 17;46(19):7767-81. doi: 10.1021/ic070336a. Epub 2007 Aug 14.

Polymetallic, highly organized molecular architectures can be created by "bottom-up" self-assembly methods using ligands with appropriately programmed coordination information. Ligands based on 2,6-picolyldihydrazone (tritopic and pentatopic) and 3,6-pyridazinedihydrazone (tetratopic) cores, with tridentate coordination pockets, are highly specific and lead...

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Dey SK, Abedin TS, Dawe LN, et al. Supramolecular self-assembled polynuclear complexes from tritopic, tetratopic, and pentatopic ligands: structural, magnetic and surface studies. Inorg Chem. 2007;46(19):7767-81doi: 10.1021/ic070336a.
Dey, S. K., Abedin, T. S., Dawe, L. N., Tandon, S. S., Collins, J. L., Thompson, L. K., Postnikov, A. V., Alam, M. S., & Müller, P. (2007). Supramolecular self-assembled polynuclear complexes from tritopic, tetratopic, and pentatopic ligands: structural, magnetic and surface studies. Inorganic chemistry, 46(19), 7767-81. https://doi.org/10.1021/ic070336a
Dey, Subrata K, et al. "Supramolecular self-assembled polynuclear complexes from tritopic, tetratopic, and pentatopic ligands: structural, magnetic and surface studies." Inorganic chemistry vol. 46,19 (2007): 7767-81. doi: https://doi.org/10.1021/ic070336a
Dey SK, Abedin TS, Dawe LN, Tandon SS, Collins JL, Thompson LK, Postnikov AV, Alam MS, Müller P. Supramolecular self-assembled polynuclear complexes from tritopic, tetratopic, and pentatopic ligands: structural, magnetic and surface studies. Inorg Chem. 2007 Sep 17;46(19):7767-81. doi: 10.1021/ic070336a. Epub 2007 Aug 14. PMID: 17696336.
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The psychokinetic effect; further A.S.P.R. experiments.

The Journal of the American Society for Psychical Research

DALE LA, WOODRUFF JL.
PMID: 20295555
J Am Soc Psych Res. 1947 Apr;41(2):65-82.

No abstract available.

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DALE LA, WOODRUFF JL. The psychokinetic effect; further A.S.P.R. experiments. J Am Soc Psych Res. 1947;41(2):65-82
DALE, L. A., & WOODRUFF, J. L. (1947). The psychokinetic effect; further A.S.P.R. experiments. The Journal of the American Society for Psychical Research, 41(2), 65-82.
DALE, L A, and WOODRUFF, J L. "The psychokinetic effect; further A.S.P.R. experiments." The Journal of the American Society for Psychical Research vol. 41,2 (1947): 65-82.
DALE LA, WOODRUFF JL. The psychokinetic effect; further A.S.P.R. experiments. J Am Soc Psych Res. 1947 Apr;41(2):65-82. PMID: 20295555.
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Showing 1 to 12 of 180 entries