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Journal articles on the topic 'Polyaza macrocycles'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Majoral, Jean Pierre, Meryam Badri, Anne Marie Caminade, Michel Delmas, and Antoine Gaset. "Reactivity of polyaza diphosphorus macrocycles." Inorganic Chemistry 30, no. 2 (1991): 344–46. http://dx.doi.org/10.1021/ic00002a039.

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2

Qian, Ligang, Zhong Sun, Mathias P. Mertes, and Kristin Bowman Mertes. "Synthesis of selectively protected polyaza macrocycles." Journal of Organic Chemistry 56, no. 16 (1991): 4904–7. http://dx.doi.org/10.1021/jo00016a018.

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3

Ren, Tong. "Sustainable metal alkynyl chemistry: 3d metals and polyaza macrocyclic ligands." Chemical Communications 52, no. 16 (2016): 3271–79. http://dx.doi.org/10.1039/c5cc09365a.

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4

Moon, Dohyun, Yong Pyo Hong, and Jong-Ha Choi. "Spectroscopic characterization and molecular structure of 3,14-dimethyl-2,6,13,17-tetraazapentacyclo[16.4.0.12,17.16,13.07,12]tetracosane." Acta Crystallographica Section C Structural Chemistry 72, no. 9 (2016): 701–4. http://dx.doi.org/10.1107/s2053229616013280.

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Constrained cyclam derivatives have been found to exhibit anti-HIV effects. The strength of binding to the CXCR4 receptor correlates with anti-HIV activity. The conformation of the macrocyclic compound is very important for co-receptor recognition. Therefore, knowledge of the conformation and crystal packing of macrocycles has become important in developing new highly effective anti-HIV drugs. Structural modifications of N-functionalized polyaza macrocyclic compounds have been achieved using various methods. A new synthesis affording single crystals of the title tetraazapentacyclo[16.4.0.12,17

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5

Chavez, F., and A. D. Sherry. "A simplified synthetic route to polyaza macrocycles." Journal of Organic Chemistry 54, no. 12 (1989): 2990–92. http://dx.doi.org/10.1021/jo00273a046.

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6

MAJORAL, J. P., M. BADRI, A. M. CAMINADE, M. DELMAS, and A. GASET. "ChemInform Abstract: Reactivity of Polyaza Diphosphorus Macrocycles." ChemInform 22, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199119222.

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7

Kovacs, Zoltan, and A. Dean Sherry. "pH-Controlled Selective Protection of Polyaza Macrocycles." Synthesis 1997, no. 07 (1997): 759–63. http://dx.doi.org/10.1055/s-1997-1418.

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8

Radecka-Paryzek, Wanda. "Self-assembly in Schiff base lanthanide complexes — From supramolecular dimers to coordination polymers." Canadian Journal of Chemistry 87, no. 1 (2009): 1–7. http://dx.doi.org/10.1139/v08-109.

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A review is given of the latest contribution of the author’s research group to the coordination chemistry of Schiff base polyaza macrocycles and acyclic salicylaldimines. Focus is placed on the effectiveness of lanthanides in supramolecular self-assembly of the components leading to the formation of compounds with unusual properties and structures.Key words: Schiff base macrocycles, salicylaldimines, lanthanides, self-assembly, template synthesis.

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9

Bernhardt, Paul V., and Geoffrey A. Lawrance. "Complexes of polyaza macrocycles bearing pendent coordinating groups." Coordination Chemistry Reviews 104, no. 2 (1990): 297–343. http://dx.doi.org/10.1016/0010-8545(90)80045-u.

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10

QIAN, L., Z. SUN, M. P. MERTES, and K. BOWMAN MERTES. "ChemInform Abstract: Synthesis of Selectively Protected Polyaza Macrocycles." ChemInform 22, no. 52 (2010): no. http://dx.doi.org/10.1002/chin.199152236.

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11

Bradshaw, Jerald S., Krzysztof E. Krakowiak, Haoyun An, and Reed M. Izatt. "A new synthetic route to polyaza-crown macrocycles through the per(N-formyl)polyaza-crowns." Journal of Heterocyclic Chemistry 29, no. 6 (1992): 1429–32. http://dx.doi.org/10.1002/jhet.5570290610.

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12

KOVACS, Z., and A. D. SHERRY. "ChemInform Abstract: pH-Controlled Selective Protection of Polyaza Macrocycles." ChemInform 28, no. 49 (2010): no. http://dx.doi.org/10.1002/chin.199749179.

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13

Kataky, Ritu, Karen E. Matthes, Patrick E. Nicholson, David Parker, and Hans-J. Buschmann. "Synthesis and binding properties of amide-functionalised polyaza macrocycles." Journal of the Chemical Society, Perkin Transactions 2, no. 8 (1990): 1425. http://dx.doi.org/10.1039/p29900001425.

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14

Radecka-Paryzek, Wanda, Violetta Patroniak, and Jerzy Lisowski. "Metal complexes of polyaza and polyoxaaza Schiff base macrocycles." Coordination Chemistry Reviews 249, no. 21-22 (2005): 2156–75. http://dx.doi.org/10.1016/j.ccr.2005.02.021.

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15

BERNHARDT, P. V., and G. A. LAWRANCE. "ChemInform Abstract: Complexes of Polyaza Macrocycles Bearing Pendent Coordinating Groups." ChemInform 22, no. 7 (2010): no. http://dx.doi.org/10.1002/chin.199107292.

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16

Izatt, R. M., R. L. Bruening, B. J. Tarbet, et al. "Macrocycle-metal cation interactions involving polyaza macrocycles bonded to silica gel via a nitrogen donor atom." Pure and Applied Chemistry 62, no. 6 (1990): 1115–18. http://dx.doi.org/10.1351/pac199062061115.

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17

Fuji, Kaoru, Kiyosei Takasu, Hisashi Miyamoto, Kiyoshi Tanaka, and Tooru Taga. "Polyaza macrocycles containing the piperazine ring as a semi-flexible moiety." Tetrahedron Letters 37, no. 39 (1996): 7111–14. http://dx.doi.org/10.1016/0040-4039(96)01586-9.

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18

Lennon, Patrick J., Hayat Rahman, Karl W. Aston, Susan L. Henke, and Dennis P. Riley. "New conformationally constrained polyaza macrocycles prepared via the bis(chloroacetamide) method." Tetrahedron Letters 35, no. 6 (1994): 853–56. http://dx.doi.org/10.1016/s0040-4039(00)75981-8.

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19

Jacques, Vincent, Mohammed Mesbahi, Verica Boskovic, and Jean F. Desreux. "Synthesis of Bicyclic Polyaza Polycarboxylic Macrocycles Containing a 12-Membered Unit." Synthesis 1995, no. 08 (1995): 1019–26. http://dx.doi.org/10.1055/s-1995-4043.

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20

Wainwright, Kevin P. "ChemInform Abstract: Applications for Polyaza Macrocycles with Nitrogen-Attached Pendant Arms." ChemInform 33, no. 50 (2010): no. http://dx.doi.org/10.1002/chin.200250235.

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21

Kataky, Ritu, David Parker, Andrew Teasdale, Jonathan P. Hutchinson, and Hans-J. Buschmann. "Binding properties of amide and amide–ester N-functionalised polyaza macrocycles." J. Chem. Soc., Perkin Trans. 2, no. 8 (1992): 1347–51. http://dx.doi.org/10.1039/p29920001347.

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22

Majoral, Jean Pierre, Meryam Badri, Anne Marie Caminade, Michel Delmas, and Antoine Gaset. "Facile synthesis of new classes of free and complexed polyaza phosphorus macrocycles." Inorganic Chemistry 27, no. 21 (1988): 3873–75. http://dx.doi.org/10.1021/ic00294a042.

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23

Burguete, M. Isabel, M. Paz Clares, Enrique García-España, Santiago V. Luis, Manel Querol, and Vicente Martí-Centelles. "Azonia spiro polyaza macrocycles containing biphenyl subunits as anion and cation receptors." Tetrahedron 67, no. 25 (2011): 4655–63. http://dx.doi.org/10.1016/j.tet.2011.04.071.

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24

Jacques, Vincent, and Jean F. Desreux. "Kinetically and thermodynamically stable isomers of thorium chelates of polyaza polycarboxylic macrocycles." Journal of Alloys and Compounds 213-214 (October 1994): 286–89. http://dx.doi.org/10.1016/0925-8388(94)90917-2.

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25

Macartney, Donal H., and Samuel Mak. "Kinetics of electron-transfer reactions of the Co(bpyO2)32+/3+ couple in acetonitrile." Canadian Journal of Chemistry 70, no. 1 (1992): 39–45. http://dx.doi.org/10.1139/v92-008.

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The kinetics of the outer-sphere electron transfer reactions of tris(1,1′-dioxo-2,2′-bipyridine)cobalt(II) and (III) with a series of nickel polyaza macrocycles, FeL3n+ and OsL32+ complexes (L is 2,2′-bipyridine or 1,10-phenanthroline, and substituted derivatives), and Rh2(O2CCH3)4(CH3CN)2+ have been investigated in acetonitrile at 25.0 °C. An application of the Marcus theory relationship to the cross-reaction rate constants yielded apparent Co(bpyO2)32+/3+ self-exchange rate constants of 102 M−1 s−1 from the nickel macrocycle cross-reactions and 10−1 M−1 s−1 from the cross-reactions with the

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26

Delgado, Rita, J. J. R. Fraústo Da Silva, M. T. S. Amorim, M. F. Cabral, Sílvia Chaves, and Judite Costa. "Dissociation constants of Br∅nsted acids in D2O and H2O: studies on polyaza and polyoxa-polyaza macrocycles and a general correlation." Analytica Chimica Acta 245 (1991): 271–82. http://dx.doi.org/10.1016/s0003-2670(00)80232-9.

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27

Rastogi, Ankur, and Ram Nayan. "Studies on copper(II) complexes of some polyaza macrocycles derived from 1,2-diaminoethane." Journal of Coordination Chemistry 62, no. 20 (2009): 3366–76. http://dx.doi.org/10.1080/00958970903062046.

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28

JACQUES, V., M. MESBAHI, V. BOSKOVIC, and J. F. DESREUX. "ChemInform Abstract: Synthesis of Bicyclic Polyaza Polycarboxylic Macrocycles Containing a 12-Membered Unit." ChemInform 26, no. 51 (2010): no. http://dx.doi.org/10.1002/chin.199551201.

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29

FUJI, K., K. TAKASU, H. MIYAMOTO, K. TANAKA, and T. TAGA. "ChemInform Abstract: Polyaza Macrocycles Containing the Piperazine Ring as a Semi-Flexible Moiety." ChemInform 28, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.199701213.

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30

KATAKY, R., D. PARKER, A. TEASDALE, J. P. HUTCHINSON, and H. J. BUSCHMANN. "ChemInform Abstract: Binding Properties of Amide and Amide-Ester N-Functionalized Polyaza Macrocycles." ChemInform 23, no. 48 (2010): no. http://dx.doi.org/10.1002/chin.199248223.

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31

Mateus, Pedro, Luís M. P. Lima, and Rita Delgado. "Di- and trinuclear copper(II) complexes of polyaza macrocycles and cryptands as anion receptors." Polyhedron 52 (March 2013): 25–42. http://dx.doi.org/10.1016/j.poly.2012.07.073.

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32

Bila, N., E. Merciny, and J. Fuger. "Determination des constantes de stabilite des complexes des lanthanides trivalents avec les macrocycles polyaza polycarboxyliques." Analytica Chimica Acta 221 (1989): 325–36. http://dx.doi.org/10.1016/s0003-2670(00)81969-8.

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33

Jazwinski, Jaroslaw, Jean-Marie Lehn, Robert Méric, et al. "Polyaza-macrocycles of cyclophane type: Synthesis, structure of a chloroform inclusion complex and anion binding." Tetrahedron Letters 28, no. 30 (1987): 3489–92. http://dx.doi.org/10.1016/s0040-4039(00)96334-2.

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34

Habibi, D., and V. Izadkhah. "SYNTHESIS OF THE NEW SCHIFF BASE POLYAZA MACROCYCLES AND THEIR COMPLEXES WITH Cu2+AND Ni2+." Phosphorus, Sulfur, and Silicon and the Related Elements 179, no. 6 (2004): 1197–202. http://dx.doi.org/10.1080/10426500490459830.

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35

Kodama, Mutsuo, Anung Budhi Mahatma, Toru Koike, and Eiichi Kimura. "The Electrochemical Study of Ag(II) Complexes of Polyaza Macrocycles and Their Acetic Acid Derivatives." Bulletin of the Chemical Society of Japan 63, no. 10 (1990): 2803–8. http://dx.doi.org/10.1246/bcsj.63.2803.

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36

Averin, A. D., A. V. Shukhaev, A. K. Buryak, and I. P. Beletskaya. "Synthesis of polyaza macrocycles by palladium-catalyzed amination of 1,2-dibromobenzene and 2-bromo-1,3-dichlorobenzene." Russian Journal of Organic Chemistry 45, no. 9 (2009): 1353–64. http://dx.doi.org/10.1134/s1070428009090085.

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37

BRADSHAW, J. S., K. E. KRAKOWIAK, H. AN, and R. M. IZATT. "ChemInform Abstract: A New Synthetic Route to Polyazacrown Macrocycles Through the Per(N- formyl)polyaza-crowns." ChemInform 24, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199318242.

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38

LENNON, P. J., H. RAHMAN, K. W. ASTON, S. L. HENKE, and D. P. RILEY. "ChemInform Abstract: New Conformationally Constrained Polyaza Macrocycles (IV) and (V) Prepared via the Bis(chloroacetamide) Method." ChemInform 25, no. 25 (2010): no. http://dx.doi.org/10.1002/chin.199425160.

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39

Mateus, Pedro, Luis M. P. Lima, and Rita Delgado. "ChemInform Abstract: Di- and Trinuclear Copper(II) Complexes of Polyaza Macrocycles and Cryptands as Anion Receptors." ChemInform 44, no. 25 (2013): no. http://dx.doi.org/10.1002/chin.201325195.

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40

BAYADA, A., G. A. LAWRANCE, M. MAEDER, and M. A. O'LEARY. "ChemInform Abstract: Metal-Directed Synthesis of Aminobenzyl Polyaza Macrocycles: Candidates for Attachment to Polymers and Biomolecules." ChemInform 26, no. 15 (2010): no. http://dx.doi.org/10.1002/chin.199515197.

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41

Averin, A. D., A. V. Shukhaev, A. K. Buryak, and I. P. Beletskaya. "ChemInform Abstract: Synthesis of Polyaza Macrocycles by Palladium-Catalyzed Amination of 1,2-Dibromobenzene and 2-Bromo-1,3-dichlorobenzene." ChemInform 41, no. 11 (2010): no. http://dx.doi.org/10.1002/chin.201011173.

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42

Borsarelli, Claudio D., Silvia E. Braslavsky, Marı́a Teresa Indelli, and Franco Scandola. "Photophysics of supercomplexes. A laser-induced optoacoustic study of the adducts between Ru(bpy)(CN)42− and polyaza macrocycles." Chemical Physics Letters 317, no. 1-2 (2000): 53–58. http://dx.doi.org/10.1016/s0009-2614(99)01360-3.

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43

Padilla-Tosta, Miguel E., José Manuel Lloris, Ramón Martínez-Máñez, et al. "Fluorescent Chemosensors for Heavy Metal Ions Based on Bis(terpyridyl) Ruthenium(II) Complexes Containing Aza-Oxa and Polyaza Macrocycles." European Journal of Inorganic Chemistry 2001, no. 6 (2001): 1475–82. http://dx.doi.org/10.1002/1099-0682(200106)2001:6<1475::aid-ejic1475>3.0.co;2-n.

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44

Gao, You-Liang, Cheng-Yu Shen, Yin-Yan Tang, Qin-Hui Luo, and Shu-Yan Yu. "A Study on Some Copper (II) Complexes of Polyaza Cryptands and Planar Macrocycles-Synthesis, Characterization and Superoxide Dismutase Activity." Chinese Journal of Chemistry 19, no. 5 (2010): 468–74. http://dx.doi.org/10.1002/cjoc.20010190507.

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45

Spirlet, Marie-Rose, Jean Rebizant, Pierre P. Barthélemy, and Jean F. Desreux. "The X-ray structure of 1,4,8,11-tetraazacyclotetradecane-1,4,8,11-tetraacetic acid and its relevance to the protonation of polyaza polycarboxylic macrocycles." J. Chem. Soc., Dalton Trans., no. 9 (1991): 2477–81. http://dx.doi.org/10.1039/dt9910002477.

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46

Arán, Vicente J., Manoj Kumar, José Molina, et al. "Synthesis and Protonation Behavior of 26-Membered Oxaaza and Polyaza Macrocycles Containing Two Heteroaromatic Units of 3,5-Disubstituted Pyrazole or 1-Benzylpyrazole. A Potentiometric and1H and13C NMR Study." Journal of Organic Chemistry 64, no. 17 (1999): 6135–46. http://dx.doi.org/10.1021/jo981699i.

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47

Aran, Vicente J., Manoj Kumar, Jose Molina, et al. "ChemInform Abstract: Synthesis and Protonation Behavior of 26-Membered Oxaaza and Polyaza Macrocycles Containing Two Heteroaromatic Units of 3,5-Disubstituted Pyrazole or 1-Benzylpyrazole. A Potentiometric and 1H and 13C NMR Study." ChemInform 31, no. 1 (2010): no. http://dx.doi.org/10.1002/chin.200001191.

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48

Zhong, Di-Chang, and Tong-Bu Lu. "Molecular recognition and activation by polyaza macrocyclic compounds based on host–guest interactions." Chemical Communications 52, no. 68 (2016): 10322–37. http://dx.doi.org/10.1039/c6cc03660k.

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49

Hosseini, Mir Wais, Jacques Comarmond, and Jean-Marie Lehn. "Synthesis of Polyaza Macrocyclic Ligands Incorporating Pyridine Units." Helvetica Chimica Acta 72, no. 5 (1989): 1066–77. http://dx.doi.org/10.1002/hlca.19890720525.

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50

Kiss, Tamas, István Lázár, and Pawel Kafarski. "Chelating Tendencies of Bioactive Aminophosphonates." Metal-Based Drugs 1, no. 2-3 (1994): 247–64. http://dx.doi.org/10.1155/mbd.1994.247.

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Abstract:

The metal-binding abilities of a wide variety of bioactive aminophosphonates, from the simple aminoethanephosphonic acids to the rather large macrocyclic polyaza derivatives, are discussed with special emphasis on a comparison of the analogous carboxylic acid and phosphonic acid systems. Examples are given of the biological importance of metal ion – aminophosphonate interactions in living systems, and also of their actual and potential applicability in medicine.

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