IL Origins What Were ILs? ILs and Green Chemistry What Are ILs
Transcription
IL Origins What Were ILs? ILs and Green Chemistry What Are ILs
5/16/2015 Are Alternative Solvent Systems such as Ionic Liquids Green or not Based on Toxicity, Chemical or Energy Use, or Utilization? (Hint: It Depends) Robin D. Rogers Canada Excellence Research Chair in Green Chemistry and Green Chemicals Department of Chemistry McGill University Montreal, QC, Canada IL Origins What Were ILs? ILs and Green Chemistry What Are ILs? ILs as Solvents ILs as Materials ILs as Pharmacueticals ILs and Innovation 1 5/16/2015 What are Ionic Liquids Anyway? Ionic Liquids Are: ♦ Toxic ♦ Expensive ♦ An Academic Curiosity ♦ Green ♦ Edible ♦ Biosourced ♦ Magic 2 5/16/2015 Perhaps Better to Ask, What were Ionic Liquids? A Short Ionic Liquid History 3 5/16/2015 Paul von Walden Bull. Acad. Impér. Sci. St. Pétersbourg, 1914, 8, 405-422 The First IL? [EtNH3][NO3] mp 12 °C 1914 Frank Hurley and Thomas Wier (Rice Institute) [1] [2] [3] [4] Hurley, F.H., Electrodeposition of aluminum, U.S. Pat., 4,446,331 (1948). Hurley, F.H. and Wier, T.P., “The electrodeposition of aluminium from nonaqueous solutions at room temperature”, J. Electrochem. Soc. 98, 207-212 (1951). Hurley, F.H. and Wier, T.P., “Electrodeposition of metals from fused quaternary ammonium salts”, J. Electrochem. Soc. 98, 203-206 (1951). Wier Jr., T.P. and Hurley, F.H., U.S. Pat., 4,446,349 (1948). 1948-51 4 5/16/2015 Bob Osteryoung, Bernard Gilbert, et al. [1] Chum, H.L., Koch, V.R., Miller, L.L. and Osteryoung, R.A., “An electrochemical scrutiny of organometallic iron complexes and hexamethylbenzene in a room temperature molten salt”, J. Am. Chem. Soc. 97, 3264-3265 (1975). [2] Koch, V.R., Miller, L.L. and Osteryoung, R.A., “Electroinitiated Friedel-Crafts transalkylations in a room-temperature molten-salt medium”, J. Am. Chem. Soc. 98 (17), 5277-5284 (1976). [3] Gilbert, R.J. and Osteryoung, R.A., “Raman spectra of molten aluminium chloride: 1-butylpyridinium chloride systems at ambient temperatures”, Inorg. Chem. 17, 27282729 (1978). 1975-78 Chuck Hussey and John Wilkes Wilkes, J.S., Levisky, J.A., Wilson, R.A. and Hussey, C.L. “Dialkylimidazolium chloroaluminate melts - a new class of room-temperature ionic liquids for electrochemistry, spectroscopy, and synthesis” Inorg. Chem. 21 (3), 1263-1264 (1982). 1982 5 5/16/2015 John Wilkes and Mike Zaworotko Wilkes, J.S. and Zaworotko, M.J. “Air and water stable 1-ethyl-3-methylimidazolium based ionic liquids,” J. Chem. Soc., Chem. Commun. (13), 965967 (1992). 1992 Chauvin Nobel Address 2005 6 5/16/2015 The First Philosophy of Ionic Liquids The general picture of these organic salts at low temperatures (below, or around 100 ºC) corresponds to the experiences made with inorganic (single, noncomplexing) molten salts at much higher temperatures (ca. 300-600 ºC). NaCl 800 oC 40 oC [C10mim][PF6] IL Definitions: low melting salts 7 5/16/2015 800 oC NaCl “The important thing in science is not so much to obtain new facts as to discover new ways of thinking about them.” Sir William Bragg British physicist (1862 - 1942) Liquid Salts that can be used as solvents Water Ionic Liquid that won’t evaporate or burn and can be immiscible with water! 8 5/16/2015 So What Were Ionic Liquids? – Low melting organic salt – Little/no vapor pressure – Non-flammable Cations – Typically has wide liquid range R5 R2 R3 R1 N + N R5 R4 R4 + R3 N – Viscous – Solvent properties are different to molecular solvents – Solvent properties can be varied (and controlled) Anions Cl-/[AlCl3] R6 Cl , Br , I R1 [NO3]-, [SO4]2- R2 - - Reactive to water - Air and water stable [CF3COO]-, [CF3SO2][BF4]- R1 N R2 R4 R3 R1 P R2 R4 R3 [PF6]- Decreasing coordinating ability Increasing hydrophobicity [CF3SO2)2N] Where did the connection between Ionic Liquids and Green Chemistry start and what happened? 9 5/16/2015 Principles of Green Chemistry • The use of auxiliary substances (e.g., solvents, separation agents, etc.) should be made unnecessary wherever practicable, and in cases where they are necessary, should be innocuous. P. T. Anastas, J. C. Warner, Green Chemistry: Theory and Practice, Oxford University Press, New York, 1998. Chemical Releases by Industry Sector a: b: c: d: e: 1,000 800 600 f: g: h: i: j: 400 200 0 a b c d e f g h i chemicals primary metals paper (multiple codes) transportation equipment plastics fabricated metals petroleum furniture printing j 10 5/16/2015 Chemical ReleasesSurface Water (2.9%) In 1994, 2.3 billion pounds of ca. 300 Toxic Release Inventory (TRI) chemicals were reported as released to the environment by TRI-reporting facilities. Air (68.9%) Land (12.8%) Underground Injection (15.4%) Motivation/Green Chemistry Non-volatile ILs can eliminate THE major pathway to environmental chemical release. 11 5/16/2015 •Crete 2000 In 2000, a group of scientists and engineers met to plan a research agenda for this growing field. Green Industrial Applications of Ionic Liquids A NATO Advanced Research Workshop Crete, Greece - April 12-16, 2000 The first international meeting dedicated to the study and application of RTIL (ambient temperature melts). 12 5/16/2015 Green Industrial Applications of Ionic Liquids A NATO Advanced Research Workshop Crete, Greece - April 12-16, 2000 Green Industrial Applications of Ionic Liquids • NATO Science Series, II/92 • From NATO Advanced Research Workshop, April1216, 2000, Heraklion, Crete. 13 5/16/2015 Green Industrial Applications of Ionic Liquids A NATO Advanced Research Workshop Crete, Greece - April 12-16, 2000 Outcomes IL are intrinsically interest and worthy of study for advancing science (ionic vs. molecular solvents) with the expectation that something useful may be derived. Combined with green chemistry, a new paradigm in thinking about synthesis in general, IL provide an opportunity for science/engineering/business to work together from the beginning of the fields' development. What was Driving This Activity? Generation 1: ILs with unique tunable physical properties Physical property R1 R4 N R1 R2 R3 N R4 P - melting point - density - viscosity - thermal stability - conductivity - hydrophobicity - refractive index R2 R3 N O N R N N F3C S Physical property O N O S CF3 O lower melting point / hydrophobicity C6H13 C6H14 P C14H29 NC N CN C6H14 hydrophobicity / lower viscosity - melting point - density F 3C - viscosity - thermal stability NC - conductivity - hydrophobicity - refractive index S O N O N S N N N N FeCl4 CN high thermal stability / hydrophilicity S O HO S O O O O O O BF4 O O Cl Cl CF3 O O OH N O S O PF6 O SOLVENTS 14 5/16/2015 Using Unusual IL Solubility/Solvation for Sustainable Technology ♦ Many ILs are water soluble and can also dissolve waterinsoluble compounds. ♦ Products can be recovered by precipitation using water as an anti-solvent. Ionic Liquid Solvents Ionic Liquids are able to dissolve biopolymers cellulose chitin 15 5/16/2015 But, the attention was on how ILs can really be used as reaction media. ILs – Common Advantages ♦ Safety – Many ILs are non-flammable and have low volatility. ♦ Environmental Impact – Low volatility of many ILs averts this release pathway and facilitates recycling. ♦ Wide liquid range – ILs allow excursions into temperatures and pressures inaccessible for many solvents. ♦ Tunability – Changing one of the ions preserves some chemical function while greatly changing the physical properties. 16 5/16/2015 ILs – Common(ly Perceived) Disadvantages ♦ Not always safe – ILs can be toxic, flammable, or explosive. ♦ Low volatility can be a disadvantage – ILs are incompatible with common evaporative methods of product isolation. ♦ Physical properties – ILs tend to be more viscous than organic solvents and may be supercooled at room temperature. ♦ Expensive – Probably the most cited drawback to ILs. “Typical” IL Ions Cations Anions Drawbacks of some ions synonymous with ILs include high cost and presence of fluoride. 17 5/16/2015 What about ‘[Bmim][PF6] 1-butyl-3-methylimidazolium hexafluorophosphate [C4mim][PF6] ♦ Was widely studied for a range of applications: electrochemistry, separations (aqueous/IL, scCO2/IL), and chemical reactions ♦ Reasons for choice ♦ ♦ ♦ ♦ ♦ ♦ widely used within peer group hydrophobic [PF6]- anion is non-coordinating easy to prepare (chloro- and bromobutane are not volatile, IL separates from water) Supercritical CO2 is soluble in [C4mim][PF6] Miscibility with ethanol in [Cnmim][PF6] varies with water Hexafluorophosphate anions are unacceptable in water! ♦ The hexafluorophosphate anion is known to be hydrolytically unstable, releasing HF on decomposition ♦ Why should this be different in an IL? ♦ Decomposition can cause dissolution of glass flasks or damage to steel autoclaves and reactors ♦ Do [PF6]- ILs have a use? Yes, mostly in primary research 18 5/16/2015 What About ILs and Toxicity? Ionic Liquids and C. elegans A Study in Toxicity (2004) 19 5/16/2015 Lethality and Aversion Alkyl chain increase lethality increases When animals are exposed to 1.0 mg/mL ionic liquid the lethality •0.0% C4mimCl •11% C8mim •97% C14mimCl Likewise the trend continues with 5.0 mg/mL ionic liquid exposure 1.0 2.5 5.0 •1.0% C4mim •66% C8mim •100% C14mim Swatloski, R. P.; Holbrey, J. D.; Memon, S. B.; Caldwell, G. A.; Caldwell, K. A.; Rogers, R. D. Chem.Commun. 2004, 6, 668-669 Preliminary Results on Other ILs 80 N + N CH 3 Cl N + N CH 3 B r N CH N + 2 F 3 F B LC50 (mg/mL) F 60 N N + CH F F F 3 P F N N N 20 HO F F N + 40 F CH N + N N + CH 3 6 7 N + 5 Cl- 3 CH 8 3 N 0 N Compound Number Toxicity Category Very highly toxic Highly toxic Moderately toxic Slightly toxic Not acutely toxic N + 14 7 2 8 10 1 3 9 13 12 11 4 5 6 B r + N B r LC50 (mg/mL) < 10-4 10-4 – 10-3 10-3 – 10-2 10-2 – 10-1 > 10-1 + N CH N + B r 3 F N CH F B 3 F F O N + N 10 O S O O 14 20 5/16/2015 Finding the RIGHT Ionic Liquid GRAS/Biologically Derived IL Ions ♦ More to the point – ILs do not need to be made out of a specific set of ions at all. ♦ Many solid compounds on food additive/Generally Recognized as Safe lists have been incorporated into ILs: ♦ Choline ♦ Small carboxylic acids ♦ Most biogenic amino acids ♦ Active pharmaceutical ingredients ♦ Biosourced ions 21 5/16/2015 Ionic Liquids Are: ♦ Toxic ♦ Expensive ♦ An Academic Curiosity ♦ Green ♦ Edible ♦ Biosourced ♦ Magic – but not one ionic liquid has all these properties! 22 5/16/2015 and, Green is in the eye of the beholder 1-Butyl-3Himidazolium Nitrate Overgeneralizations and The Green Counter-Revolution Oversimplification in reports on ILs as solvents led to a host of studies cautioning against their application in green chemistry. 23 5/16/2015 Overgeneralizations Can Be Misleading Benzene is carcinogenic (expensive/toxic/fill-in-the-blank) = ALL ‘solvents’ are carcinogenic (expensive/toxic/fill-in-the-blank) Water is green (cheap/nontoxic/___) = ALL ‘solvents’ are green (cheap/nontoxic/___) A Few Cations and Anions now found in Ionic Liquids N N N N N N N NH2 NC N NC N NH2 N NO2 H2 N N N N P O N C N N N S N S C N N O C N I- S NO2 N N N Br- Cl- N O2N N N F F O F C O N NO2 N N N O2N O2N N N N N F F O F S O O F F F N F F F F F S O2N O O F N O S N O O N N NO2 N O S O S O N H2N O N F N F F F O F F B F F F F P O B F F O N F N F3 C O N O CF2 F O B O F P F CF3 C O F2 C F B C CF3 O F F2 F F F3 C 2 O O O2N N 24 5/16/2015 Dual-functionality Imparts a Unique Architectural Platform The chemist has independent design control via modification of either the cation, the anion, or both. Parent cation Structural modification to cation Parent anion Combination of functionalized anion and cation Multifunctional ionic liquid composed of independently designed components Structural modification to anion ILs are a platform strategy to deliver different chemical and physical functionality in the same compound, but segregated into different ion components; this has applicability in many different materials areas, but is currently underutilized. 25 5/16/2015 What Are Ionic Liquids? Nonvolatile monopropellant for advanced propulsion systems1 Room-temperature liquid dual biological action for pharmaceutical applications2 Magnetically responsive liquid crystal for advanced displays3 Ionic liquids are tools for unlocking new technologies 1. Shamshina, J. L.; Smiglak, M.; Drab, D. M.; Parker, T. G.; Dykes, H. W. H., Jr.; Di Salvo, R.; Reich, A. J.; Rogers, R. D. Chem. Commun. 2010, 46, 8965. Bica, K.; Rijksen, C.; Nieuwenhuyzen, M.; Rogers, R. D. Phys. Chem. Chem. Phys. 2010, 12, 2011. Getsis, A.; Balke, B.; Felser, C.; Mudring, A. –V. Crys. Growth Des. 2009, 9, 4429. 2. 3. Generation 1: ILs with unique tunable physical properties Physical property R1 R1 - melting point - density R4 N R2 R4 P R2 - viscosity R3 R3 - thermal stability ILs with targeted chemical - conductivity N N - hydrophobicity Chemical Nproperty - refractive index R OH N N N N O OEt N N N N N N N N n SO3H N CN - chemical N reactivity - high energy density - electrochemical window - flammability - coordination - solvation - chiral induction O N N F3C Physical property O S N O S CF3 O lower melting point / hydrophobicity Generation 2: C 6H13 NC CNwith properties combined C6H14 P C14H 29 N C6H14 hydrophobicity /Olower viscosity N N NO2 2N N - melting point O O Cl - density F3C S N S CF3 - viscosity O O - thermal FeCl4 stability NC properties CN chosen physical O - conductivity N BF4 - hydrophobicity HO S O O Chemical property - refractive index O N O NCl N NN N energy density / oxygen balance high thermal stability / hydrophilicity N N Cl lower density / solvation N N N N O F3C OEt O S O O N S O N O2N CF3 O OH O - high energy O S N O N PF6 S density O COO O O - electrochemical H CN window N - flammability N N I CO - oxygen balance Rh - UV blocker I CO NC CN - chiral induction - solvation Cl N NO2 COO N chiral induction/ hydrophobicity An Example: ENERGETIC MATERIALS 26 5/16/2015 Ideal IL Energetic Material: Desired Properties Physical Properties Melting point < -40 °C Surface tension < 100 dyne cm-1 Density > 1.4 g cm-3 Viscosity As low as possible Hazard Sensitivity Thermal stability TGA (75 °C, < 1% loss of material isothermal) over 24 h TGA (rate 10oC/min) > 120 °C for Tdecomp Thermodynamic properties Heat of formation as positive as possible Heat of combustion > 6 kcal g-1 Impact > 50 kg cm Friction Detonation Electrostatic discharge > 120 N LD50 > 0.5 g kg-1 > 5000 V at 0.25 J AMES Negative Toxicology Independent, Modular Design of Components in Multifunctional EILs Project Goal To develop synthetic strategies for the introduction of energetic functions and components into potential ionic liquids (IL) and to determine the resultant physical properties. Targeted Properties Cation Anion New Energetic IL Materials Utilizing IL Tools New, functionalized material Cation Anion New Synthesis and Properties • Drab, D. M.; Smiglak, M.; Rogers, R. D. Chim. Oggi 2006, 24, 27. • Smiglak, M.; Metlen, A.; Rogers, R. D. Acc. Chem. Res., 2007, submitted. 27 5/16/2015 Endless possibilities – Azolium Azolates Cations NH2 N N N N N H2N N N N NH2 N NO2 CN N N N N NH2 N N N N N NH2 OH N N O2N O2 N NO2 N O2N N N NC N O 2N N N N NC N N NO2 NC N N N N NC O2N N NO2 N N N N NO2 N O2N N NH2 N N N N N O2N N NO2 O 2N O2N NO2 N O2N N Anions N3 N N N N N NH2 NC N NC N O2 N N N N NO2 N O2N N N O2N N N Examples of possible ions for use in formation of azolium azolate EILs. ILs as Hypergols • ILs with certain anions have been reported to hypergolic with a variety of oxidizers Clark, J. D. Ignition: An Informal History of Liquid Rocket Propellants, Rutgers University Press, New Brunswick, NJ, 1972. Schneider et al. Energy Fuels 2008, 22, 2871-2872. 56 28 5/16/2015 Boron NPs Enhance Hypergolic Properties [C4mim][DCA] B NPs milled in [MAT][DCA] [MAT][DCA] B NPs milled in [MAT][DCA] 57 NC O2 N N N NC N N N N N NH2 N N NC N NC N NH2 N NO2 N H2N N N N P N S N H3C N N C N N N N HO S C CH3 N N O N S O C N N F F O F C O H3C O Cellulose Solvent Physical: Low Melting Salts N F F O F S O NO2 O N N O2N N N O2N F F F N N F F F F F O N F S O N S 2 O N O N O O O S O N N NO2 N S O N F F H2N O F N F O N F B F N N F N O F N B O F P F N F N F O F N O F3C CF2 F O B O F F P CF3 O O F B C CF3 C F2C F F F F2 2 F3C O N O O2N O2N N N O2N N N O N I- N NO2 N Br- Cl- N N N N O2N N NO2 N N Energetic Material Chemical: High Energy Content 29 5/16/2015 Generation 1: ILs with unique tunable physical properties Physical property R1 R1 R4 N R2 R4 P R3 N - melting point - density - viscosity - thermal stability - conductivity - hydrophobicity - refractive index R2 R3 N N R O N N F3C Physical property O S N S O CF3 O lower melting point / hydrophobicity C6H13 C6H14 P C14H29 NC CN N C6H14 hydrophobicity / lower viscosity - melting point - density F3 C - viscosity - thermal stability NC - conductivity - hydrophobicity - refractive index O S O N S O N FeCl4 CN O BF4 HO O S O O O OH Cl CF3 O O O What Is The Next Step In The Evolution of Ionic Liquids? N N N N N Cl S O high thermal stability / hydrophilicity O O S PF6 O O Generation 2: ILs with targeted chemical properties combined with chosen physical properties Chemical property Chemical property N N O OEt N N N N N N N N n SO3H N CN - chemical reactivity - high energy density - electrochemical window - flammability - coordination - solvation - chiral induction N N N N NO2 N energy density / oxygen balance N N Cl lower density / solvation N N N O2N N N N O F3C OEt O S O O N S O OH - high energy density - electrochemical window - flammability - oxygen balance - UV blocker - chiral induction - solvation Cl N I CO CN N N N I NC N O2N CF3 N COO H N Rh CO CN NO2 COO N chiral induction/ hydrophobicity 30 5/16/2015 Can Toxicity be Useful? • Previous literature has shown that ionic liquids can possess biological activity • Also others have used biologically active ions in the synthesis of ionic liquids • Typically, however, these ionic liquids did not focus on the biological property but the ability of the ions to form ionic liquids 1. Pernak, A., Iwanik, K., Majewski, P., Grzymislawski, M., & Pernak, J. Ionic liquids as an alternative to formalin in histopathological diagnosis, Acta Histochemica, 107(2), 149-156 (2005). 2. Pernak, J., Sobaszkiewicz, K., & Mirska, I., Anti-microbial activities of ionic liquids, Green Chem., 5(1), 52-56 (2003) 3. Nockemann, P., Thijs, B., Driesen, K., Janssen, C., Van Hecke, K., Van Meervelt, L., Kossmann, S., Kirchner, B., Binnemans, K., J. Phys. Chem. B, 111(19), 5254-5263 (2007) ILs as Poisons? Theophrastus Paracelsus (14931541) “All things are poison and nothing is without poison, only the dose permits something not to be poisonous.” Circa Survive “The Difference Between Medicine and Poison is in the Dose” (2007) from On Letting Go Image: http://en.wikipedia.org/wiki/Paracelsus; http://en.wikipedia.org/wiki/Circa_Survive 31 5/16/2015 Biological Activity? Generation 3: ILs with targeted biological properties combined with chosen physical and chemical properties O O Biological property n=14 Biological property N COO n=5-15 anti-bacterial / UV blocker NH COO n O Ph HO Ph - emollient - anti-acne H2N - antibiotic - non-steroidal anti-inflammatory drug (NSAID) - vitamin N O3S O n=7 O n lower melting, antibacterial / NSAID O COO O S N O COO O O O n=7 n n O NH N local anesthetic / emollient N n=5-15 n O O - antibacterial - local anesthetic - anticholinergic - antifungal n N O NH Why not consider, biological activity, as the primary IL property and look at ILs as APIs? n N O3S NH Ph O NH H S N O O COO Hough, W. H.; Smiglak, M.; Rodríguez, H.; Swatloski, R. P.; Spear, S. K.; Daly, D. T.; Pernak, J.; Grisel, J. E.; Carliss, R. D.; Soutullo, M. D.; Davis, Jr., J. H.; Rogers, R. D. “The Third Evolution of Ionic Liquids: Active Pharmaceutical Ingredients,” New J. Chem. 2007, 31, 1429-1436. Ionic Liquids as Active Pharmaceutical Ingredients (APIs) 32 5/16/2015 We have proposed, that in addition to the traditional crystalline salt screening and selection that most pharmaceuticals undergo, that pure liquid salt forms of APIs should be considered as a design strategy to overcome potential problems such as polymorphism, solubility, and bioavailability. Stoimenovski et al. “Crystalline vs. Ionic Liquid Salt Forms of Active Pharmaceutical Ingredients: A Position Paper,” Pharm. Res. 2010, 27, 521. O NH O O N O n n = 10 (2-acetoxyethyl)dodecyloxymethyldimethylammonium Anti-bacterial NH O Lidocainium Pain Reliver N n n = 14 Hexadecylpyridinium n Anti-bacterial n=9 (2-hydroxyethyl)undecyloxymethyldimethylammonium Anti-bacterial OH N n n=7 Didecyldimethylammonium Anti-bacterial O O N O O O (2-acetoxyethyl)heptyloxymethyldimethylammonium Anti-bacterial O NH S N Sulfathiazole Antibacterial O O O NH O O O N S O O NH Naproxenate 2 Cinnamate Sulfacetamide Anti-Inflammatory UV Blocker O Antibacterial O OH Cl SO3 O NH n O n Cl n=7 O Colawet MA-80 Wetting Agent NH O O O O NH O Diclofenac Anti-Inflammatory O SO3 N S O O Acesulfamate Artifical Sweetener Ibuprofenate Anti-Inflammatory O n n = 5 to 15 NO2 Ranitidinium Histamine H2-receptor antagonist O O S N N S NH2 N Benzalkonium Anti-bacterial NH O O Hg Thimerosal Preservative O Docusate Emollient Mepenzolate Anticholinergic n n=5 S O OH N O O SO3 O n O O N O S O O OH O Salicylate Saccharinate Artifical Sweetener Anti-Acne N n n = 5 to 15 O O IL-API: Lidocainium Docusate IL-API: Benzalkonium Cinnamate Biological: Hydrophobic Pain Reliever Biological: Anti-Bacterial Sunscreen 33 5/16/2015 ILs - Tools and Strategies Easy modification of Physical Properties Ionic Liquid Toolbox H3C N N N N N N F F F F P F F Tuning of Hydrophobicity/ Lipophilicity O O NO2 N N N F F N HF N N N O F P 2 F F O2N N NO2 O2N N N O n N O2N n n=7 NH2 Oligomers NO2 O O O N N N N O S N O Dual Functionality NO2 Dissolution O O Physical properties ♦ Ionic Liquid formation will influence the physical properties of a solid drug. Polymorphism Solid drug Ionic Liquids Toxicity Stability Dissolution rate Solubility Permeability Bioavailability 34 5/16/2015 Ionic Liquid ToolBox Approach O O3S O O O O O Sodium Docusate Emollient N n n = 5 to 15 Sodium Ibuprofenate Anti-Inflammatory O N S O O Lidocaine HCl Pain Reliever O O NH H 2N Benzalkonium Chloride Sodium Sulfacetamide Anti-Bacterial Anti-Acne O -O S 3 O O O S H N H N Ranitidine HCl NO2 Histamine H2-receptor Antagonist n Colawet MA-80 Wetting Agent H N HN N n n=7 Didecyldimethylammounium Chloride Anti-Bacterial Overcoming Polymorphism: Ranitidine Docusate O H3C H2 NH C H3C O H2 H2 H2 C S C C NH NH CH3 O3S O O CHNO2 O Form Dark Red Liquid Melting Point Liquid at R.T. Tg (glass transition) -12 °C Thermal Stability T5%onset = 163 °C, Tonset = 249 °C, Tdec = 278 °C • Anti-ulcer drug (Zantac™) by GlaxoSmithKline • Subject of litigation over polymorphic forms and purity1 1. Goho, A. “The crystal form of a drug can be the secret to its success.” Science News <http://www.sciencenews.org/articles/20040821/bob9.asp> (2004). 35 5/16/2015 Tuning of Hydrophobicity/ Lipophilicity Hydrophobicity/Lipophilicity ♦ Ion pairing with appropriate counterions increases hydrophobicity and lipophilicity of the API which could tune solubility and bioavailability. Hydrophilicity Lipophilicity Hydrophobicity 36 5/16/2015 Dual Functionality Dual functionality ♦ Ionic Liquids can be composed of 2 active ions with complimentary functions or even the possibility of synergistic effects. Active Cation + • • • • • • • • Local anaesthetics & Analgesics Antibacterials /antiparasitics Antiemetics Stimulants /appetite suppressants Antiarrhythmics Vitamins Antimalarias Chemotherapeutics Active Anion – NSAIDs Emollients Vitamins Sweeteners UV protectors Penetration enhancers • Antivirals • • • • • • 37 5/16/2015 Dual Functionality N O n n = 5 to 15 antibacterial, hydrophobic N O Antiinflammatory, hydrophilic n n = 5 to 15 O O [Benzalkonium][Ibuprofenate] Anti-bacterial + Anti-Inflammatory, yellow gel, mp -41 °C, glass transition -77 °C Aspirin Ionic liquid salt forms of aspirin and its main metabolite salicylic acid can be prepared with pharmaceutically active cations. 38 5/16/2015 Antibacterial (1, 2, 3, 4, 5), analgesic (6), local anesthetic (7, 8) and antiarrhythmic (9) cations used in combination with the salicylate (a) and acetylsalicylate anion (b) Bica, K.; Rijksen, C.; Nieuwenhuyzen, M.; Rogers, R. D. “In Search of Pure Liquid Salt Forms of Aspirin: Ionic Liquid Approaches with Acetylsalicylic Acid and Salicylic Acid,” Phys. Chem. Chem. Phys. 2010, 12, 2011-2017. A DISRUPTIVE TECHNOLOGY? One Dual Drug, Liquid Salt! New, patentable material of matter, as well as new formulation and use patents Current Industry Practice - Compounding: Drug A + Drug B In One Pill Old Paradigm: B Not a new material of matter, only formulation or use patents possible 39 5/16/2015 Dual Functionality – Are there any Commercial Applications? (Press Release, May 26th, 2009, MEDRx Co.) ♦ Patent Application: “Tape Preparation Comprising Etodolac in Ionic Liquid Form” (Priority Date: December 11th, 2007) ♦ Etodolac patch now under Phase III clinical trial ♦ In March 2011, KOWA Company and MedRx signed an agreement that gives KOWA exclusive sales rights in in US and Commonwealth of Puerto Rico to sell the etodolac patch (http://www.medrx.co.jp/english/newsrelease.html, last accessed 05-06-12) ….but let’s expand our thinking a bit into not so well defined areas… 40 5/16/2015 Oligomers: a liquifaction and dosing strategy Oligomeric ions • Hydrogen-bonded oligomeric ions in ILs can expand the liquid range and modify properties of a salt. – Reduced melting point or glass transition temperature – Reduced viscosity – Individual dosing of 2 or more active compounds in one liquid formulation 41 5/16/2015 Confused Ionic Liquid Ions – A “Liquification” and Dosage Strategy for Pharmaceutically Active Salts The liquid and compositional ranges of ionic liquids, specifically pharmaceutically active ionic liquids, can be expanded by simple mixing with a solid acid or base to form oligomeric ions. Bica, K.; Rogers, R. D. “Confused Ionic Liquid Ions – A “Liquification” and Dosage Strategy for Pharmaceutically Active Salts,” Chem. Commun. 2010, 46, 1215. DSC Evidence 42 5/16/2015 Oligomeric ions - Examples • Lidocaine salicylate: local anaesthetic & NSAID Lid:Sal 3:1, 2.5:1, 2:1, 1.5:1, 1:1, 1:1.5, 1:2, 1:2.5, 1:3 Oligomeric Ions - Tools It is important to note that the concept of oligomeric ions enables liquefaction of solid ILs (or other salts) by simply changing the stoichiometry or complexity of the ions and the strategy need not employ the parent of the anion or cation in use. 43 5/16/2015 Liquid Engineering? Liquid Formulation via Grinding ♦ Liquid formulations can be obtained by simple grinding of 2 solid materials Grinding H N N O OH O Lidocaine mp 68 °C [Lidocaine][Decanoic acid] Tg - 38 °C Decanoic acid mp 36 °C 44 5/16/2015 Lidocaine Stearates vs. Lidocaine Decanoates Lidocaine Oleates Phase Diagram of Lidocaine Oleic acid Melting Point, oC 80 60 40 20 0 “Deep Eutectic Region” -20 -40 -60 -80 0.0 0.2 0.4 0.6 0.8 1.0 Mol Fraction lidocaine 45 5/16/2015 Liquid Co-Crystals ♦ While ILs are often considered to have weak intermolecular interactions, the melting point of lidocaine oleate is reduced by forming a strongly associated acid-base pair Lidocaine Oleate Bica, K.; Shamshina, J. L.; Hough, W. L.; MacFarlane, D. R.; Rogers, R. D. Chem. Commun. 2010, 47, 2267-2269. Lidocaine Oleate – Ionic Liquid or Eutectic? Hydrogen bonding Mixture Complete or partial ionization Ionic liquid Is this ‘pure’ hydrogen bonding which persists in solution? Bica, K.; Shamshina, J.; Hough. W. L.; MacFarlane, D. R.; Rogers, R. D. “Liquid Forms of Pharmaceutical Co-crystals: Exploring the Boundaries of Salt Formation,” Chem. Commun. 2011, 47, 2267-2269. 46 5/16/2015 Or is it partial ionization and strong interaction? Lidocaine Ibuprofen ♦ Synthesis ♦ Characterization ♦ Membrane transport Lidocaine & Ibuprofen Partial Ionization? Hydrogen bonding Mixture Complete or partial ionization Ionic liquid Where is the proton in these liquids? 47 5/16/2015 Synthesis of [Lid]m[Ibu]n Lidocaine Ibuprofen + grinding mp: 68 ºC mp: 76 ºC Lidocaine ibuprofen ([Lid]m[Ibu]n) Enhanced Membrane Transport 48 5/16/2015 Membrane transport Membrane transport: a technique to measure the permeation of drugs through the skin. Lidocaine Ibuprofen ([Lid][Ibu]) Tetrabutylphosphonium Ibuprofen ([P4444][Ibu]) Tg: -26 ºC Ephedrine Ibuprofen ([Eph][Ibu]) Tg: -43 ºC mp: 110 ºC Experimental Setup Goal: To test the membrane transport ability of IL-APIs Franz cell: Donor solution: APIs in ethanol, propylene glycol solution, or neat IL-APIs +‒‒+ ‒+ + ‒ ‒+ + + ‒ ‒ ‒ ‒ Silicone membrane Sample collecting port + + ‒ + After sample collection, fresh, prewarmed and degassed PBS were injected. Phosphate Buffered Saline (PBS) 49 5/16/2015 Membrane transport Neutral compounds Donor solutions: APIs/EtOH, 0.5 mmol/mL Commercial salts ♦ Membrane transport decreases in the order: neutral compounds > ILAPIs > commercial salts. ♦ [Lid][Ibu] permeates the membrane faster than the other two salts, [Eph][Ibu] and [P4444][Ibu]. Membrane Transport ♦ The transport ability of partially ionized IL-APIs through the model silicone membrane is shown to be higher than their corresponding commercial drugs, suggesting that IL-APIs can change the bioavailability of orally delivered APIs. ♦ Neat liquid IL-APIs could readily transport through the membrane, in the absence of any solvents. 50 5/16/2015 BUT … There are a Few Disadvantages of the ‘Liquid’ Form … Liquid form ♦ The ‘liquid’ property can have a negative impact on: ♦ Ease of preparation ♦ Handling and use ♦ Special devices for dosing and administration Solids Handling of Ionic Liquids 51 5/16/2015 When an Ionic Liquid is on a Solid Support … Supported Ionic Liquid Phases (SILPs) ♦ SILPs have been successfully used for immobilization of transition metal catalysts (heterogenous catalysis as hydroformylation1) 1Riisager et al. Eur. J. Inorg. Chem. 2006, 695. IL-APIs Used an active anion paired with an “ionic liquid maker” cation two active ions combined in a weakly ionized ionic liquid 52 5/16/2015 How are SILPs Made? Porous network SILP catalyst particle Ionic liquid film Solid Carrier Solid support Solid carriers - any inorganic or carbon support (e.g. mesoporous silica) combines the advantages of IL-APIs with the advantages of a solid drug form. Improved Handling ♦ Liquid state properties have significant impact on ease of preparation and handling compared to solid drugs and need of special devices for dosing and administration. ♦ By supporting the IL-APIs on solid carrier, an easier way to handle and dose is provided. ♦ Due to the mesoporous structure of the used silica, the adsorbed ionic liquid can be obtained as solid material even in high loading of 50% (wt/wt). 10, 20, and 50% [wt/wt] [P4444][Ibu] on SiO2-90 53 5/16/2015 Controlled Release? (Please pay attention to the different X-axis scales) PBS (pH = 7.4) SGF (pH = 6.8) 250 Concentration (ppm) 200 150 100 50 [P4444][Ibu], 20% 250 [P4444][Ibu], 20% [LidI][bu], 20% 200 Concentration (ppm) 250 Concentration (ppm) SIF (pH = 1.2) 150 100 50 200 150 100 50 [Lid][Ibu], 20% [Lid][Ibu], 20% 0 0 0 0 10 20 30 40 50 60 [P4444][Ibu], 20% 70 0 60 Time (min) 120 180 240 300 0 10 20 30 40 50 60 70 80 90 100 Time (min) Time (min) O P HO O O H H N O [P4444][Ibu] N [Lid][Ibu] Pharmaceutically Active Ionic Liquids with Solids Handling, Enhanced Thermal Stability, and Fast Release Katharina Bica, Héctor Rodríguez, Gabriela Gurau, O. Andreea Cojocaru, Anders Riisager, Rasmus Fehrmann, and Robin D. Rogers* (Chem. Comm., 2012, 48, 5422-5424.) ♦ Biologically active ionic liquids supported on mesoporous silica provide solid handling with fast and complete release in an aqueous environment. 54 5/16/2015 Application of Ionic Liquids in the Pharmaceutical Industry Separation Drug extraction Drug detection Crystallization ILs Solvents Active pharmaceutical ingredients (APIs) Will Ionic Liquids be transformational? Ionic Liquids for Solubilization (Hydrotropes) ♦ ILs can be used as solvents for hard-to-dissolve actives ♦ Tunable properties of ILs for specific dissolution ♦ Simple modification of HLB (Hydrophilic - Lipophilic Balance) of ILs by choice of ions HLB-IL McCrary, P. D.; Beasley, P. A.; Gurau, G.; Narita, A.; Barber, P. S.; Cojocaru, A.; Rogers, R. D. “Drug specific, tuning of an ionic liquid’s hydrophilic–lipophilic balance to improve water solubility of poorly soluble active pharmaceutical ingredients,” New J. Chem. 2013, 37, 2196-2202. 55 5/16/2015 IL Design Strategy Amphotericin B – 1.0 ng/mL Itraconazole – 0.2 µg/mL Left: [OAc]- based ILs to dissolve Amp B by tuning cation hydrophobicity; Right: PEG-based ILs with a hydrophilic cation and tunable hydrophobicity in the anion to dissolve itraconazole. ILs to Dissolve Amp B Solubility dominated by H-bonding Hydrophilic portion Hydrophobic portion – 15 C-C bonds ♦ [OAc]- was chosen as the hydrophilic anion due to its ability to dissolve cellulose by preferentially hydrogen bonding with cellulose molecules.1 ♦ A cation was chosen to pair with [OAc]- to allow for flexibility in design tuning the IL’s overall HLB to match the structure of Amp B 1 – Swatloski, R. P.; Spear, S. K.; Holbrey, J. D.; Rogers, R. D. J. Am. Chem. Soc. 2002, 124, 4974-4975. 56 5/16/2015 HLB Balance through a lipophilic amine Alkyl chain length designed to properly match the structure of Amp B Amp B dissolved in [C6NH3][OAc] 5 mg/mL 10 mg/mL 20 mg/mL 30 mg/mL 50 mg/mL 57 5/16/2015 IL solution is loaded into water ♦ For example, using 10 mg of Amp B/mL of [C6NH3][OAc] stock solution, aliquots of the stock solution are dissolved in water. Concentration in mg Amp B per mL of HexOAc Concentration of mg Amp B in H2O Enhanced solubility only observed by first dissolving Amp B in the IL. Starting from 10 mg/mL 0.50 mg/mL 0.01 mg/mL 0.25 mg/mL 1 mg/mL 0.10 mg/mL Not Soluble Soluble! Soluble for 1 min 58 5/16/2015 Ionic Liquids Are: ♦ Magic Because they make you think and allow you to dream…. Green Quest Robin D. Rogers Canada Excellence Research Chair in Green Chemistry and Green Chemicals Department of Chemistry McGill University 59 5/16/2015 Tuscaloosa, AL USA to Montreal, Canada 2199.83 km / 22 h 1 min Green Chemistry Green Chemistry is more than designing new chemical products and processes that are sustainable, Green Chemistry represents new business opportunities that are sustainable. 60 5/16/2015 An Introduction to George Washington Carver •Tuscaloosa Don’t be distracted from special opportunities by “Green Chemistry” or by over emphasis on “Reaction Media”! 61 5/16/2015 Utilizing Ionic Liquids and Green Chemistry for Sustainable Technology Through Innovation BIOMASS MATERIALS BIO-ACTIVE MATERIALS The use of Ionic Liquids Technology as a basis for the design, development, and delivery of biologically active ingredients: • Active Pharmaceutical Ingredients (APIs) • Nutraceuticals • Agrochemicals (pesticides, herbicides, fungicides) SEPARATIONS IONIC LIQUIDS polymeric and composite materials from biorenewable polymers BIO-ACTIVE MATERIALS BIOMASS Addressing a DOE Grand Challenge through Ionic Liquids Technology ENERGETICS Sustainability tunable properties by design and choice of ions ACTINIDES ENERGETICS possible combinations for dual functional Ionic Liquids Use the tunability of Ionic Liquids to find safe synthetic routes to ILs with high energy content and targeted physical and chemical properties, to replace currently in use energetic materials. Sustainability New TechnologyNew Companies International Program ANION ACTINIDES Use of Ionic Liquids to solve fundamental and applied problems in f-element coordination chemistry and separations. Space ready propellants: Hypergolic ionic liquids with exfoliated graphene Rogers Group RESEARCH IS A CONTINUUM Where there is new knowledge, there can be innovation: Top: Coordination of uraniumselective IL. Right: renewable adsorbent fibers for extraction of uranium from seawater. CONTACT INTERNATIONAL PROGRAM Hosting international visitors through collaborative projects Institute of Process Engineering Chinese Academy of Sciences ♦ New Knowledge ♦ New Technologies China Turkey ♦ Entrepreneurs ♦ New Companies “new sustainable technologies based on the unique attributes of Ionic Liquids” Iran Prof. Robin D. Rogers [email protected] http://bama.ua.edu/~rdrogers/ We will Choose Sustainability Targets: ♦Energy ♦Water ♦Materials ♦Medicine 62 5/16/2015 We will produce technologies that are Environmentally Sustainable, Economically Sustainable, and Socially Sustainable, while developing: ♦ Entrepreneurs ♦ New Companies ♦ New Knowledge We will Let Green Chemistry Guide Our Work, not Define Us! 63 5/16/2015 Green Chemistry is less about your tool and more about what you accomplish! The Future of Ionic Liquids? OPPORTUNITY! 64