Specific Bifunctionalization on the Phosphorus Dendrimers: History
View Latest Version
Please note this is an old version of this entry, which may differ significantly from the current revision.
Contributor:
Massimo Petriccone
,
Régis Laurent
,
Cédric-Olivier Turrin
,
Rosa Maria Sebastián
,
Anne-Marie Caminade

Dendrimers are highly branched three-dimensional macromolecules, which properties are essentially dependent on the type of their terminal functions. Dendrimers are synthesized by iterative processes, which afford a new generation at the end of each sequence, characterized by a multiplication of the number of terminal functions. Such processes generate identical terminal functions on the surface of the dendrimers. However, it is sometimes desirable to have two types of surface functions in order to fulfil specific properties. Numerous properties have been explored already, most of them being related to catalysis, materials, or biology/nanomedicine. Strategies to get two types of terminal functions will be illustrated with polyphosphorhydrazone (PPH) dendrimers.

  • dendrimer
  • properties
  • bifunctionalization

1. Introduction

Dendrimers are synthesized by iterative processes, which afford a new generation at the end of each sequence, characterized by a multiplication of the number of terminal functions, most generally by two [1] or three [2], depending on the branching motives. Such processes generate identical terminal functions on the surface of the dendrimers, of course depending on the type of dendrimers, and on the synthetic process used. Such terminal functions can be modified uniformly to bring new properties. However, it is desirable in some cases to have two types of terminal functions, each type of functions affording eventually its own properties (for instance, one function for the solubility, the other affording properties for catalysis or biology, or one type of function for the grafting (for instance to materials), with the other functions bringing another property).
In most cases, the presence of two (or even more) functions on the surface of dendrimers is carried out using a stochastic approach (i.e., an uncontrolled number and location of each type of functions). However, this approach is contradictory with the aim of having a perfectly controlled and reproducible structure for the dendrimers, contrarily to classical polymers. Even if efforts have been carried out to increase the purity of compounds issued from the stochastic approach [3], batch-to -batch inconsistencies are unavoidable, and induce in particular undesirable varying biological activities [4]. To solve this type of problem, it is highly desirable to synthesize dendrimers precisely bifunctionalized on their surface. Figure 1 displays the difference between both approaches.
Organics 03 00018 g001 550
Figure 1. Examples of batches of bifunctionalized dendrimers. (A) Stochastic functionalization on the surface of dendrimers. (B) Precise bifunctionalization on the surface of dendrimers.
The easiest way to get dendrimers specifically bifunctionalized on their surface consists in grafting on each terminal function a compound bearing already both desired functions (Scheme 1A). Such a method has been applied to different types of dendrimers and functions. One can cite for instance as an early example the presence of both a phenyl and a pyrene on the surface of a series of dendrimers built on an arylether scaffold, and used for studying charge-transfer processes from the core to the surface [5]. More recent examples concern PAMAM (polyamidoamine) dendrimers functionalized with different aminoacids, to have NH2 groups together with either OH, SH, or other functional groups, and tested for drug delivery [6]. Polyester dendrimers functionalized with both OH and azide, used later on in click chemistry to afford biosensors ,[7] or functionalized with both azide and alkyne, as a multipurpose platform, in particular to afford implant adhesives in bone fracture applications [8] are other more recent examples. Azide alkyne monomeric compounds have been used for synthesizing by click chemistry multifunctional nanocarriers bearing as terminal functions a model drug (R-lipoic acid), a fluorescent dye (BODIPY), and a poly(ethylene glycol) (PEG) chain [9]. Other recent examples of grafting directly two functions concern PPI (polypropyleneimine) dendrimers functionalized with both an electroactive carbazole and a mesogenic unit, all dendrimers of this family being liquid crystalline [10], and also Newkome-type polyamide dendrimers, functionalized with both one azide and two olefins .[11] A series of bifunctional dendrimers has been obtained from either a polyester-polyamide, or polyester-lysine, or polyamine-lysine hybrid internal structure functionalized on the surface with orthogonally protected aspartic acid [12]. The selective and sequential deprotection of the amine and of the carboxylic acid of the protected aspartic acid was carried out to graft a long PEG (115 units in average), and either a gadolinium complex [13],[14] or diverse other lanthanide complexes (Dy, Yb [15], Eu, and Sm [16]) for magnetic resonance imaging (MRI), or two synthetic tubulysin analogues against C26 colon carcinomas [17]. Lysine derivatives protected by two different protecting groups, were grafted on the surface of lysine dendrimers and dendrons. Selective deprotection afforded dendrimers bearing both gadolinium complexes and PEG as MRI contrast agents [18]. The same process was applied to a series of dendrons having a carboxylic acid at the core and both a gadolinium complex and galactosyl moieties on the surface, as liver targeting imaging probes [19]. Another lysine-dendron bearing a long PEG chain at the core (114 units in average) and both a porphyrin analogue and cholic acid, was used for near-infrared fluorescence imaging (NIRFI), magnetic resonance imaging (MRI), positron emission tomography (PET) and dual modal PET-MRI [20].
Organics 03 00018 sch001 550
Scheme 1. Schematization of the different methods used for having precisely two types of different functions on the surface of dendrimers. (A) grafting on each terminal function a compound bearing already both desired functions. (B) modifying one function already on the surface, to generate two functions. (C) sequential grafting of one function, followed by the grafting of the second one.
Other methods to get two types of terminal functions have been very rarely used. One can cite the possibility to modify one function already on the surface, to generate two functions (Scheme 1B). Such type of reaction has been illustrated with functionalized amines used for opening cyclic carbonates on the surface of polyester dendrimers [21].
The last method concerns the sequential grafting of one function, followed by the grafting of the second one, as illustrated in Scheme 1C. Such a type of reaction is rare, and has been used essentially with dendrimers having dichlorotriazine as terminal functions, reacted in sequential nucleophilic aromatic substitution with two different amines [22]. MRI (Magnetic Resonance Imaging) contrast agents have been obtained in this way, one amine bearing a ligand suitable for complexing gadolinium, the other an alcohol [23].
Besides the different types of dendrimers indicated above, another type of dendrimer is known for the versatility of its chemistry, namely phosphorus dendrimers, and particularly polyphosphorhydrazone (PPH) dendrimers, which possess a phosphorus atom at each branching point [24]. They are generally built from either P(S)Cl3 or hexachlorocyclotriphosphazene as core [25]. Their structure is illustrated in Figure 2 with the first and second generations. Both generations are displayed as the full chemical structure, but also in a linear form with parentheses after each layer of branching points. The presence of either P(S)Cl2 or aldehyde terminal functions, depending on the step considered, enables a versatile reactivity to fulfil the desired properties.
Organics 03 00018 g002 550
Figure 2. Two ways for drawing the 1st and 2nd generations of polyphosphorhydrazone dendrimers: full chemical structure, and linear structure with parenthesis after each layer of branching points.

2. Sequential Grafting of a First, then a Second Function on the Surface of PPH Dendrimers

As indicated in the introduction, sequential grafting on the surface of dendrimers, as shown in Scheme 1C, is very rare, and has been carried out only and recently with triazine dendrimers [22,23]. On the contrary, such a type of reaction is carried out since a long time with polyphosphorhydrazone dendrimers, thanks to the specific reactivity of the P(S)Cl2 terminal functions. The possibility of such sequential reaction was discovered first with secondary amines. Indeed, only one Cl of each P(S)Cl2 terminal functions was able to react with diallylamine (even when used excessively). However, the remaining Cl was able to react with primary amines, such as propargylamine (Scheme 2). This sequential reaction is not limited to secondary amines. Indeed, depending on the conditions used (temperature and quantity of amine), it is possible to react only one allylamine on each P(S)Cl2 terminal function. Some reactions were carried out up to the seventh generation [26].
Organics 03 00018 sch016 550
Scheme 2. Sequential addition of two different amines on the surface of PPH dendrimers.
In some cases, the surface functions are P(O)Cl2 instead of P(S)Cl2, but they display the same specific reactivity. In particular, one propargylamine or one allylamine could be grafted on each P(O)Cl2 function. As in the previous case, the second reaction can be carried out with propargylamine when allylamine was already grafted (Scheme 3) [26].
Organics 03 00018 sch017 550
Scheme 3. Sequential addition of two different amines on the surface of polyphosphorhydrazone dendrimers having P(O)Cl2 terminal functions.
The same type of reaction was carried out more recently to obtain compounds bearing both a triethoxysilane and a primary amine. Boc-monoprotected ethylene diamine as the amino part, and 3-(triethoxysilyl) propylamine as the silyl part were chosen. The first step was the grafting of one of the two amines (way a or way b, Scheme 4), followed by the grafting of the other amine in the second step, affording the same compound in both cases. Besides, a large excess of 1,3-diaminopropane can be used as the second amine, to directly afford a free amine as terminal function (Scheme 4) [27]. These compounds were tested among other dendritic structures possessing both types of functions for the grafting to silica, followed by attempts for trapping CO2, after deprotection of the Boc-protected amine, to form a carbamate. These compounds having both types of functions on the surface were not the most efficient. Indeed, dendrons possessing a single triethoxysilyl group at the core and several primary amines on the surface were found to be more efficient [28].
Organics 03 00018 sch018 550
Scheme 4. Other examples of sequential addition of two different amines on PPH dendrimers, to be grafted to silica, and used for trapping CO2.
Besides the grafting of two amines, it is also possible to graft both an amine and a phenol. Such type of reaction was carried out up to now only on P(O)Cl2 terminal functions. After the grafting of either allyl amine or propargylamine, the second step was the grafting of 4-hydroxybenzaldehyde, in basic conditions. The aldehydes were then used for the condensation with hydrazine in large excess, or for Wittig reactions with the ylide Ph3P=CH-C≡N (Scheme 5) [26]. Hydroxybenzaldehyde could react also when bulky diallylamine was grafted in the first step [29].
Organics 03 00018 sch019 550
Scheme 5. Sequential addition of an amine and of 4-hydroxybenzaldehyde on the surface of PPH dendrimers.
The presence of the aldehydes as shown in Scheme 5 enabled the continuation of the synthesis of dendrimers having pendant internal functions inside the structure. These pendant groups were either an allylamine, or 1-aminomethylpyrene, or 1-pyrenebutanoic hydrazide. The aldehydes were reacted with H2NNMeP(S)Cl2, as in the classical synthesis of PPH dendrimers (Scheme 6) [30].
Organics 03 00018 sch020 550
Scheme 6. Amino derivatives of allyl or pyrene as pendant functions inside polyphosphorhydrazone dendrimers.
Besides the sequential use of two amines, or of an amine and a phenol shown in the previous Schemes, the sequential use of two phenols was also attempted on the surface of polyphosphorhydrazone dendrimers. The reaction is less clean than with amines, as it is difficult to avoid a small percentage (less than 5%) of either homodisubstitution, or unreacted P(S)Cl2. The grafting of a phenol derivative of ethacrynic acid, followed by the grafting of either 4-hydroxybenzaldehyde or the phenol of the azabisphosphonate were carried out (Scheme 7). Ethacrynic acid grafted on the entire surface of phosphorhydrazone dendrimers was shown to display strong anti-proliferative activities against both liquid and solid tumors [31]. However, these unsymmetrical compounds were not tested [32].
Organics 03 00018 sch021 550
Scheme 7. Grafting of a phenol derivative of ethacrynic acid and other phenols on the surface of PPH dendrimers having anticancer properties.
In conclusion, the specific bifunctionalization on the surface of dendrimers is still an ongoing challenge. Despite being challenging, the specific presence of two functions on the surface of dendrimers offers new opportunities for the future, in particular for increasing the solubility in specific media such as water and for dendrimers having catalytic or biological properties. In this regard, efforts should be engaged to develop efficient new strategies leading to sophisticated and highly controlled multifunctional dendrimeric architectures.

This entry is adapted from the peer-reviewed paper 10.3390/org3030018

References

  1. Newkome, G.R.; Shreiner, C.D. Poly(amidoamine), Polypropylenimine, and Related Dendrimers and Dendrons Possessing Different 1 → 2 Branching Motifs: An overview of the Divergent Procedures. Polymer 2008, 49, 1–173. https://doi.org/10.1016/j.polymer.2007.10.021.
  2. Newkome, G.R.; Shreiner, C. Dendrimers Derived from 1 → 3 Branching Motifs. Chem. Rev. 2010, 110, 6338–6442. https://doi.org/10.1021/cr900341m.
  3. Mullen, D.G.; Borgmeier, E.L.; Desai, A.M.; van Dongen, M.A.; Barash, M.; Cheng, X.M.; Baker, J.R.; Holl, M.M.B. Isolation and Characterization of Dendrimers with Precise Numbers of Functional Groups. Chem. –A Eur. J. 2010, 16, 10675–10678. https://doi.org/10.1002/chem.201001175.
  4. Thomas, T.P.; Huang, B.H.; Choi, S.K.; Silpe, J.E.; Kotlyar, A.; Desai, A.M.; Zong, H.; Gam, J.; Joice, M.; Baker, J.R. Polyvalent Dendrimer-Methotrexate as a Folate Receptor-Targeted Cancer Therapeutic. Mol. Pharm. 2012, 9, 2669–2676. https://doi.org/10.1021/mp3002232.
  5. Thomas, K.R.J.; Thompson, A.L.; Sivakumar, A.V.; Bardeen, C.J.; Thayumanavan, S. Energy and Electron Transfer in Bifunc-tional Non-Conjugated Dendrimers. J. Am. Chem. Soc. 2005, 127, 373–383. https://doi.org/10.1021/ja044778m.
  6. Navath, R.S.; Menjoge, A.R.; Wang, B.; Romero, R.; Kannan, S.; Kannan, R.M. Amino Acid-Functionalized Dendrimers with Heterobifunctional Chemoselective Peripheral Groups for Drug Delivery Applications. Biomacromolecules 2010, 11, 1544–1563. https://doi.org/10.1021/bm100186b.
  7. Montanez, M.I.; Hed, Y.; Utsel, S.; Ropponen, J.; Malmstrom, E.; Wagberg, L.; Hult, A.; Malkoch, M. Bifunctional Den-dronized Cellulose Surfaces as Biosensors. Biomacromolecules 2011, 12, 2114–2125. https://doi.org/10.1021/bm200201y.
  8. Hed, Y.; Oberg, K.; Berg, S.; Nordberg, A.; von Holst, H.; Malkoch, M. Multipurpose Heterofunctional Dendritic Scaffolds as Crosslinkers towards Functional Soft Hydrogels and Implant Adhesives in Bone Fracture Applications. J. Mater. Chem. B 2013, 1, 6015–6019. https://doi.org/10.1039/c3tb21061h.
  9. Sharma, A.; Neibert, K.; Sharma, R.; Hourani, R.; Maysinger, D.; Kakkar, A. Facile Construction of Multifunctional Nanocarriers Using Sequential Click Chemistry for Applications in Biology. Macromolecules 2011, 44, 521–529. https://doi.org/10.1021/ma102354k.
  10. Castelar, S.; Romero, P.; Serrano, J.L.; Barbera, J.; Marcos, M. Multifunctional Ionic Hybrid Poly (propyleneimine) Den-drimers Surrounded by Carbazole Dendrons: Liquid Crystals, Optical and Electrochemical Properties. RSC Adv. 2015, 5, 65932–65941. https://doi.org/10.1039/c5ra12237f.
  11. Kaufman, E.A.; Tarallo, R.; Elacqua, E.; Carberry, T.P.; Weck, M. Synthesis of Well-Defined Bifunctional Newkome-Type Dendrimers. Macromolecules 2017, 50, 4897–4905. https://doi.org/10.1021/acs.macromol.7b01035.
  12. van der Poll, D.G.; Kieler-Ferguson, H.M.; Floyd, W.C.; Guillaudeu, S.J.; Jerger, K.; Szoka, F.C.; Frechet, J.M. Design, Syn-thesis, and Biological Evaluation of a Robust, Biodegradable Dendrimer. Bioconjugate Chem. 2010, 21, 764–773. https://doi.org/10.1021/bc900553n.
  13. Floyd, W.C.; Klemm, P.J.; Smiles, D.E.; Kohlgruber, A.C.; Pierre, V.C.; Mynar, J.L.; Frechet, J.M.J.; Raymond, K.N. Conjuga-tion Effects of Various Linkers on Gd(III) MRI Contrast Agents with Dendrimers: Optimizing the Hydroxypyridinonate (HOPO) Ligands with Nontoxic, Degradable Esteramide (EA) Dendrimers for High Relaxivity. J. Am. Chem. Soc. 2011, 133, 2390–2393. https://doi.org/10.1021/ja110582e.
  14. Klemm, P.J.; Floyd, W.C.; Smiles, D.E.; Frechet, J.M.J.; Raymond, K.N. Improving T1 and T2 Magnetic Resonance Imaging Contrast Agents through the Conjugation of an Esteramide Dendrimer to High-Water-Coordination Gd (III) Hydroxypyri-dinone Complexes. Contrast Media Mol. Imaging 2012, 7, 95–99. https://doi.org/10.1002/cmmi.483.
  15. Klemm, P.J.; Floyd, W.C.; Andolina, C.M.; Frechet, J.M.J.; Raymond, K.N. Conjugation to Biocompatible Dendrimers In-creases Lanthanide T2 Relaxivity of Hydroxypyridinone Complexes for Magnetic Resonance Imaging. Eur. J. Inorg. Chem. 2012, 2012, 2108–2114. https://doi.org/10.1002/ejic.201101167.
  16. Andolina, C.M.; Klemm, P.J.; Floyd, W.C.; Frechet, J.M.J.; Raymond, K.N. Analysis of Lanthanide Complex Dendrimer Conjugates for Bimodal NIR and MRI Imaging. Macromolecules 2012, 45, 8982–8990. https://doi.org/10.1021/ma302206g.
  17. Floyd, W.C.; Datta, G.K.; Imamura, S.; Kieler-Ferguson, H.M.; Jerger, K.; Patterson, A.W.; Fox, M.E.; Szoka, F.C.; Frechet, J.M.J.; Ellman, J.A. Chemotherapeutic Evaluation of a Synthetic Tubulysin Analogue-Dendrimer Conjugate in C26 Tumor Bearing Mice. Chem. Med. Chem. 2011, 6, 49–53. https://doi.org/10.1002/cmdc.201000377.
  18. Luo, K.; Liu, G.; She, W.C.; Wang, Q.Y.; Wang, G.; He, B.; Ai, H.; Gong, Q.Y.; Song, B.; Gu, Z.W. Gadolinium-labeled Peptide Dendrimers with Controlled Structures as Potential Magnetic Resonance Imaging Contrast Agents. Biomaterials 2011, 32, 7951–7960. https://doi.org/10.1016/j.biomaterials.2011.07.006.
  19. Luo, K.; Liu, G.; He, B.; Wu, Y.; Gong, Q.Y.; Song, B.; Ai, H.; Gu, Z.W. Multifunctional Gadolinium-based Dendritic Macro-molecules as Liver Targeting Imaging Probes. Biomaterials 2011, 32, 2575–2585. https://doi.org/10.1016/j.biomaterials.2010.12.049.
  20. Li, Y.P.; Lin, T.Y.; Luo, Y.; Liu, Q.Q.; Xiao, W.W.; Guo, W.C.; Lac, D.; Zhang, H.Y.; Feng, C.H.; Wachsmann-Hogiu, S.; et al. A Smart and Versatile Theranostic Nanomedicine Platform Based on Nanoporphyrin. Nat. Commun. 2014, 5, 4712. https://doi.org/10.1038/ncomms5712.
  21. Goodwin, A.P.; Lam, S.S.; Frechet, J.M.J. Rapid, Efficient Synthesis of Heterobifunctional Biodegradable Dendrimers. J. Am. Chem. Soc. 2007, 129, 6994–6995. https://doi.org/10.1021/ja071530z.
  22. Patra, S.; Kozura, B.; Huang, A.Y.T.; Enciso, A.E.; Sun, X.K.; Hsieh, J.T.; Kao, C.L.; Chen, H.T.; Simanek, E.E. Dendrimers Terminated with Dichlorotriazine Groups Provide a Route to Compositional Diversity. Org. Lett. 2013, 15, 3808–3811. https://doi.org/10.1021/ol400811h.
  23. Lim, J.; Turkbey, B.; Bernardo, M.; Bryant, L.H.; Garzoni, M.; Pavan, G.M.; Nakajima, T.; Choyke, P.L.; Simanek, E.E.; Koba-yashi, H. Gadolinium MRI Contrast Agents Based on Triazine Dendrimers: Relaxivity and In Vivo Pharmacokinetics. Bio-conjugate Chem. 2012, 23, 2291–2299. https://doi.org/10.1021/bc300461r.
  24. Launay, N.; Caminade, A.M.; Lahana, R.; Majoral, J.P. A General Synthetic Strategy for Neutral Phosphorus-Containing Dendrimers. Angew. Chem. Int. Edit. Engl. 1994, 33, 1589–1592. https://doi.org/10.1002/anie.199415891.
  25. Launay, N.; Caminade, A.M.; Majoral, J.P. Synthesis of Bowl-Shaped Dendrimers from Generation 1 to Generation 8. J. Or-ganomet. Chem. 1997, 529, 51–58. https://doi.org/10.1016/s0022-328x(96)06293-6.
  26. Lartigue, M.L.; Slany, M.; Caminade, A.M.; Majoral, J.P. Phosphorus-Containing Dendrimers: Synthesis of Macromolecules with Multiple Tri- and Tetrafunctionalization. Chem. –A Eur. J. 1996, 2, 1417–1426. https://doi.org/10.1002/chem.19960021114.
  27. Riegert, D.; Pla-Quintana, A.; Fuchs, S.; Laurent, R.; Turrin, C.O.; Duhayon, C.; Majoral, J.P.; Chaumonnot, A.; Caminade, A.M. Diversified Strategies for the Synthesis of Bifunctional Dendrimeric Structures. Eur. J. Org. Chem. 2013, 2013, 5414–5422. https://doi.org/10.1002/ejoc.201300456.
  28. Riegert, D.; Bareille, L.; Laurent, R.; Majoral, J.P.; Caminade, A.M.; Chaumonnot, A. Silica Functionalized by Bifunctional Dendrimers: Hybrid Nanomaterials for Trapping CO2. Eur. J. Inorg. Chem. 2016, 2016, 3103–3110. https://doi.org/10.1002/ejic.201600426.
  29. Lartigue, M.L.; Caminade, A.M.; Majoral, J.P. Synthesis and Reactivity of Dendrimers Based on Phosphoryl (P= O) Groups. Phosphorus Sulfur Silicon Relat. Elem. 1997, 123, 21–34. https://doi.org/10.1080/10426509708044195.
  30. Severac, M.; Leclaire, J.; Sutra, P.; Caminade, A.M.; Majoral, J.P. A New Way for the Internal Functionalization of Den-drimers. Tetrahedron Lett. 2004, 45, 3019–3022. https://doi.org/10.1016/j.tetlet.2004.02.120.
  31. El Brahmi, N.; Mignani, S.M.; Caron, J.; El Kazzouli, S.; Bousmina, M.M.; Caminade, A.M.; Cresteil, T.; Majoral, J.P. Investi-gations on Dendrimer Space Reveal Solid and Liquid Tumor Growth-Inhibition by Original Phosphorus-Based Dendrimers and the Corresponding Monomers and Dendrons with Ethacrynic Acid Motifs. Nanoscale 2015, 7, 3915–3922. https://doi.org/10.1039/c4nr05983b.
  32. El Brahmi, N.; El Kazzouli, S.; Mignani, S.; Laurent, R.; Ladeira, S.; Caminade, A.M.; Bousmina, M.; Majoral, J.P. Symmetrical and Unsymmetrical Incorporation of Active Biological Monomers on the Surface of Phosphorus Dendrimers. Tetrahedron 2017, 73, 1331–1341. https://doi.org/10.1016/j.tet.2017.01.044.
More
© Text is available under the terms and conditions of the Creative Commons Attribution (CC BY) license; additional terms may apply. By using this site, you agree to the Terms and Conditions and Privacy Policy.
This entry is offline, you can click here to edit this entry!
ScholarVision Creations
Feedback