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DOI: 10.1055/s-2002-32980
DABdendr as a Building Block
Publication History
Publication Date:
25 July 2002 (online)
Biographical Sketches
Introduction
Since dendrimers were first reported, by Tomalia et al., [1] researchers in the field of dendrimer science have focused primarily on the synthesis and chemical modification of these systems. At present, a wide variety of dendrimers with different properties are known [2] [3] and many of these materials contain poly(propyleneimine) dendrimers (DABdendr) as building blocks. It is well established that the physical properties of dendrimers are determined by the nature of the peripheral groups3 and, in this context, DABdendr systems have been used to prepare compounds for different applications: for example, monolayers on gold, [4] liquid crystals [5] or additives to a liquid crystal matrix, [6] dioxygen binding by copper complexes, [7] cationic dendrimers for gene delivery, [8] organometallic photonucleases, [9] carbohydrate-coated dendrimers, [10] cyclodextrin binding by cobaltocenium-functionalized dendrimers, [11] amorphous calcium carbonate stabilizers, [12] photoswitchable supramolecular systems, [13] guest molecules in encapsulation. [14]
Preparation
The first approach to the synthesis of DABdendr was reported by Vögtle. [15] However, procedures for the large-scale preparation of these materials in their different generations was first described by Wörner and Mülhaupt [16] and, independently, de Brabander-van den Berg and Meijer (in back-to-back manuscripts) in 1993. [17] The synthetic route is shown in the scheme below. Today, DABdendr materials are commercially available up to the fifth generation.
Abstracts
Dimethyldodecylammonium chloride-functionalized third generation DABdendr systems have proven to have strong anti-bacterial properties. These compounds are over two orders of magnitude more potent against Escherichia coli than their low molecular weight counterpart (n-dodecyltrimethylammonium chloride). [18] | |
Since the first report of a dendritic box, [19] the open and close control of dendrimers has been the focus of many research groups. Balzani and Vögtle [20] have described a fourth generation DABdendr bearing up to 32 photoisomerizable azobenzene groups in the periphery. These materials have been used as potential hosts for Eosin Y. The all-E azobenzene dendrimers can be reversibly switched to their Z form by light excitation. Eosin is hosted more efficiently by the dendrimers in the Z form than the E form. | |
Test experiments involving the Heck reaction have demonstrated that dendritic diphosphane palladium complexes have a significantly higher catalytic activity (typically, turnover numbers of 50 versus 16 for the parent compound). This phenomenon is attributable to the higher thermal stability of the dendritic complexes. After precipitation from the reaction mixture, the isolated Pd-containing dendrimer was reused in the same reaction and displayed comparable catalytic activity. [21] | |
DABdendr systems have been modified by the incorporation of palmityl and adamantly endgroups through either a thiourea or urea linkage. The resulting materials have been used as multivalent hosts in organic solvents for a number of guest molecules containing a terminal urea-glycine unit, with multiple secondary interactions (hydrogen and ionic bondings) being responsible for the guest-host compatibility. [22] |
- 1
Tomalia DA.Baker H.Dewald J.Hall M.Kallos G.Martin S.Roeck J.Ryeder J.Smith P. Polym. J. 1985, 17: 117 -
2a
Fischer M.Vögtle F. Angew. Chem. Int. Ed. 1999, 38: 885 -
2b
Newkome GR.Moorefield CN.Vögtle F. Dendrimers and Dendrons Wiley-VCH; Weinheim: 2001. - 3
Bosman AW.Janssen HM.Meijer EW. Chem. Rev. 1999, 99: 1665 -
4a
Noble COIV.McCarley RL. J. Am Chem. Soc. 2000, 122: 6518 -
4b
Noble COIV.McCarley RL. Org. Lett. 1999, 1: 1021 - 5
Yonetake K.Masuko T.Morishita T.Suzuki K.Ueda M. Macromolecules 1999, 32: 6578 - 6
Baars MWPL.van Boxtel MCW.Bastiaansen CWM.Broer DJ.Söntjens SHM.Meijer EW. Adv. Mater. 2000, 12: 715 - 7
Klein-Gebbink RJM.Bosman AW.Feiters MC.Meijer EW.Nolte RJM. Chem.-Eur. J. 1999, 5: 65 - 8
Ren T.Zhang G.Liu D. Tetrahedron Lett. 2001, 42: 1007 - 9
Hurley AL.Moler DL. Org. Lett. 2000, 2: 2745 - 10
Ashton PR.Boyd SE.Brown CL.Nepogodiev SA.Meijer EW.Peerlings HWI.Stoddart JF. Chem.-Eur. J. 1997, 3: 974 - 11
González B.Casado CM.Alonso B.Cuadrado I.Morán M.Wang Y.Kaifer AE. Chem. Commun. 1998, 2569 - 12
Donners JJJM.Heywood BR.Meijer EW.Nolte RJM.Roman C.Schenning APHJ.Sommerdijk NAJM. Chem. Commun. 2000, 1937 -
13a
Archut A.Vögtle F.De Cola L.Azzellini GC.Balzani V.Ramanujam PS.Berg RH. Chem.-Eur. J. 1998, 4: 699 -
13b
Archut A.Vögtle F.De Cola L.Azzellini GC.Balzani V. J. Am. Chem. Soc. 1998, 120: 12187 -
13c
Stephan H.Spies H.Johannsen B.Kauffmann C.Vögtle F. Org. Lett. 2000, 2: 2343 -
13d
Tsuda K.Gensch T.Hofkens J.Latterini L.Weener JW.Meijer EW.De Schryver FC. J. Am Chem. Soc. 2000, 122: 3445 -
13e
Dol GC.Tsuda K.Weener JW.Bartels MJ.Asavei T.Gensch T.Hofkens J.Latterini L.Schenning APHJ.Meijer EW.De Schryver FC. Angew. Chem. Int. Ed. 2001, 40: 1710 -
14a
Schenning APHJ.Elissen-Román C.Weener JW.Baars MWPL.van der Gaast SJ.Meijer EW. J. Am. Chem. Soc. 1998, 120: 8199 -
14b
Pistolis G.Malliaris A.Tsiourvas D.Paleos CM. Chem.-Eur. J. 1999, 5: 1440 -
14c
Pan Y.Ford WT. Macromolecules 2000, 33: 3731 - 15
Buhleier E.Wehner W.Vögtle F. Synthesis 1978, 155 - 16
Wörner C.Mülhaupt R. Angew. Chem., Int. Ed. Engl. 1993, 32: 1306 - 17
de Brabander-van den Berg EMM.Meijer EW. Angew. Chem., Int. Ed. Engl. 1993, 32: 1308 - 18
Chen CZ.Tan NCB.Cooper SL. Chem. Commun. 1999, 1585 - 19
Jansen JFGA.de Brabander-van den Berg EMM.Meijer EW. Science 1994, 266: 1226 - 20
Archut A.Azellini GC.Balzani V.De Cola L.Vögtle F. J. Am. Chem. Soc. 1998, 120: 12187 - 21
Reetz MT.Lohmer G.Schwickardi R. Angew. Chem., Int. Ed. Engl. 1997, 36: 1526 -
22a
Baars MWPL.Karlsson AJ.Sorokin V.de Waal BFW.Meijer EW. Angew. Chem. Int. Ed. 2000, 39: 4262 -
22b
Boas U.Karlsson AJ.de Waal BFM.Meijer EW. J. Org. Chem. 2001, 66: 2136
References
- 1
Tomalia DA.Baker H.Dewald J.Hall M.Kallos G.Martin S.Roeck J.Ryeder J.Smith P. Polym. J. 1985, 17: 117 -
2a
Fischer M.Vögtle F. Angew. Chem. Int. Ed. 1999, 38: 885 -
2b
Newkome GR.Moorefield CN.Vögtle F. Dendrimers and Dendrons Wiley-VCH; Weinheim: 2001. - 3
Bosman AW.Janssen HM.Meijer EW. Chem. Rev. 1999, 99: 1665 -
4a
Noble COIV.McCarley RL. J. Am Chem. Soc. 2000, 122: 6518 -
4b
Noble COIV.McCarley RL. Org. Lett. 1999, 1: 1021 - 5
Yonetake K.Masuko T.Morishita T.Suzuki K.Ueda M. Macromolecules 1999, 32: 6578 - 6
Baars MWPL.van Boxtel MCW.Bastiaansen CWM.Broer DJ.Söntjens SHM.Meijer EW. Adv. Mater. 2000, 12: 715 - 7
Klein-Gebbink RJM.Bosman AW.Feiters MC.Meijer EW.Nolte RJM. Chem.-Eur. J. 1999, 5: 65 - 8
Ren T.Zhang G.Liu D. Tetrahedron Lett. 2001, 42: 1007 - 9
Hurley AL.Moler DL. Org. Lett. 2000, 2: 2745 - 10
Ashton PR.Boyd SE.Brown CL.Nepogodiev SA.Meijer EW.Peerlings HWI.Stoddart JF. Chem.-Eur. J. 1997, 3: 974 - 11
González B.Casado CM.Alonso B.Cuadrado I.Morán M.Wang Y.Kaifer AE. Chem. Commun. 1998, 2569 - 12
Donners JJJM.Heywood BR.Meijer EW.Nolte RJM.Roman C.Schenning APHJ.Sommerdijk NAJM. Chem. Commun. 2000, 1937 -
13a
Archut A.Vögtle F.De Cola L.Azzellini GC.Balzani V.Ramanujam PS.Berg RH. Chem.-Eur. J. 1998, 4: 699 -
13b
Archut A.Vögtle F.De Cola L.Azzellini GC.Balzani V. J. Am. Chem. Soc. 1998, 120: 12187 -
13c
Stephan H.Spies H.Johannsen B.Kauffmann C.Vögtle F. Org. Lett. 2000, 2: 2343 -
13d
Tsuda K.Gensch T.Hofkens J.Latterini L.Weener JW.Meijer EW.De Schryver FC. J. Am Chem. Soc. 2000, 122: 3445 -
13e
Dol GC.Tsuda K.Weener JW.Bartels MJ.Asavei T.Gensch T.Hofkens J.Latterini L.Schenning APHJ.Meijer EW.De Schryver FC. Angew. Chem. Int. Ed. 2001, 40: 1710 -
14a
Schenning APHJ.Elissen-Román C.Weener JW.Baars MWPL.van der Gaast SJ.Meijer EW. J. Am. Chem. Soc. 1998, 120: 8199 -
14b
Pistolis G.Malliaris A.Tsiourvas D.Paleos CM. Chem.-Eur. J. 1999, 5: 1440 -
14c
Pan Y.Ford WT. Macromolecules 2000, 33: 3731 - 15
Buhleier E.Wehner W.Vögtle F. Synthesis 1978, 155 - 16
Wörner C.Mülhaupt R. Angew. Chem., Int. Ed. Engl. 1993, 32: 1306 - 17
de Brabander-van den Berg EMM.Meijer EW. Angew. Chem., Int. Ed. Engl. 1993, 32: 1308 - 18
Chen CZ.Tan NCB.Cooper SL. Chem. Commun. 1999, 1585 - 19
Jansen JFGA.de Brabander-van den Berg EMM.Meijer EW. Science 1994, 266: 1226 - 20
Archut A.Azellini GC.Balzani V.De Cola L.Vögtle F. J. Am. Chem. Soc. 1998, 120: 12187 - 21
Reetz MT.Lohmer G.Schwickardi R. Angew. Chem., Int. Ed. Engl. 1997, 36: 1526 -
22a
Baars MWPL.Karlsson AJ.Sorokin V.de Waal BFW.Meijer EW. Angew. Chem. Int. Ed. 2000, 39: 4262 -
22b
Boas U.Karlsson AJ.de Waal BFM.Meijer EW. J. Org. Chem. 2001, 66: 2136