Dr. Bates graduated from the University of Toledo College of Medicine in 1982. He works in Toledo, OH and specializes in Internal Medicine. Dr. Bates is affiliated with University Of Toledo Medical Center.
Kaiser Permanente Medical GroupKaiser Permanente Skyline Specialty 1375 E 20 Ave, Denver, CO 80205 3033384545 (phone), 3038613605 (fax)
Education:
Medical School Indiana University School of Medicine Graduated: 1994
Languages:
English Spanish
Description:
Dr. Bates graduated from the Indiana University School of Medicine in 1994. He works in Denver, CO and specializes in Pulmonary Disease and Sleep Medicine. Dr. Bates is affiliated with Rocky Mountain Hospital For Children, St Joseph Hospital and Swedish Medical Center.
- Pasadena CA, US Tzu-Pin LIN - Pasadena CA, US Alice CHANG - Los Angeles CA, US Hsiang-Yun CHEN - Pasadena CA, US Christopher M. BATES - Santa Barbara CA, US
In an aspect, a method of synthesizing a graft copolymer comprises the steps of: copolymerizing a first macromonomer and a first reactive diluent; wherein said first macromonomer comprises a first backbone precursor directly or indirectly covalently linked to a first polymer side chain group; wherein said reactive diluent is provided in the presence of the first macromonomer at an amount selected so as to result in formation said graft copolymer having a first backbone incorporating said diluent and said first macromonomer in a first polymer block characterized by a preselected first graft density or a preselected first graft distribution of said first macromonomer. In some embodiments of this aspect, said preselected first graft density is any value selected from the range of 0.05 to 0.75. In some methods, the composition and amount of said diluent is selected to provide both a first preselected first graft density and a first preselected first graft distribution.
Non-Aqueous Fluoride Salts, Solutions, And Their Uses
- Pasadena CA, US - TOKYO, JP Christopher M. BATES - Monrovia CA, US Nebojsa MOMCILOVIC - Vienna VA, US Brett M. SAVOIE - Pasadena CA, US Michael A. WEBB - Pasadena CA, US Robert H. GRUBBS - South Pasadena CA, US Christopher BROOKS - Dublin OH, US Kaoru OMICHI - Columbus OH, US
Assignee:
CALIFORNIA INSTITUTE OF TECHNOLOGY - Pasadena CA HONDA MOTOR CO., LTD. - TOKYO
Electrolyte solutions including at least one anhydrous fluoride salt and at least one non-aqueous solvent are presented. The fluoride salt includes an organic cation having a charge center (e.g., N, P, S, or O) that does not possess a carbon in the β-position or does not possess a carbon in the β-position having a bound hydrogen. This salt structure facilitates its ability to be made anhydrous without decomposition. Example anhydrous fluoride salts include (2,2-dimethylpropyl)trimethylammonium fluoride and bis(2,2-dimethylpropyl)dimethylammonium fluoride. Combining these fluoride salts with at least one fluorine-containing non-aqueous solvent (e.g., bis(2,2,2-trifluoroethyl)ether; (BTFE)) promotes solubility of the salt within the non-aqueous solvents. The solvent may be a mixture of at least one non-aqueous, fluorine-containing solvent and at least one other non-aqueous, fluorine or non-fluorine containing solvent (e.g., BTFE and propionitrile or dimethoxyethane). The electrolyte solutions may be employed in electrochemical cells, such as batteries, fuel cells, electrolysis systems, and capacitors.
Organic Synthesis Applications Of Non-Aqueous Fluoride Salt Solutions
- Pasadena CA, US - Oakland CA, US Christopher M. BATES - Pasadena CA, US Nebojsa MOMCILOVIC - Pasadena CA, US Brett M. SAVOIE - Pasadena CA, US Michael A. WEBB - Pasadena CA, US Robert H. GRUBBS - Pasadena CA, US Jennifer M. MURPHY - Pasadena CA, US
Assignee:
CALIFORNIA INSTITUTE OF TECHNOLOGY - Pasadena CA THE REGENTS OF THE UNIVERSITY OF CALIFORNIA - Oakland CA
Processes and reaction mixtures including non-aqueous solvent mixtures are presented. Non-aqueous solvent mixtures including fluoride salt and non-aqueous solvent combinations are provided that possess high fluoride ion concentrations useful for a range of applications, including organic synthesis. Further non-aqueous solvent mixtures are provided including a salt possessing a non-fluoride anion and a non-aqueous solvent that, when contacted with aqueous fluoride-containing reagents, extract fluoride ions to form non-aqueous fluoride-ion solutions possessing high fluoride-ion concentrations. The salts include an organic cation that does not possess a carbon in the β-position or does not possess a carbon in the β-position having a bound hydrogen. This salt structure facilitates its ability to be made anhydrous without decomposition. Example anhydrous fluoride salts include (2,2-dimethylpropyl)trimethylammonium fluoride and bis(2,2-dimethylpropyl)dimethylammonium fluoride. The combination of these fluoride salts with at least one fluorine-containing non-aqueous solvent (e.g., bis(2,2,2-trifluoroethyl)ether; (BTFE)) promotes solubility of the salt within the non-aqueous solvents.
Control Of Polymer Architectures By Living Ring-Opening Metathesis Copolymerization
- Pasadena CA, US Tzu-Pin LIN - Pasadena CA, US Alice CHANG - Los Angeles CA, US Hsiang-Yun CHEN - Pasadena CA, US Christopher M. BATES - Santa Barbara CA, US
International Classification:
C08G 81/02 C08F 267/10 C08F 285/00 C08F 287/00
Abstract:
In an aspect, a method of synthesizing a graft copolymer comprises the steps of: copolymerizing a first macromonomer and a first reactive diluent; wherein said first macromonomer comprises a first backbone precursor directly or indirectly covalently linked to a first polymer side chain group; wherein said reactive diluent is provided in the presence of the first macromonomer at an amount selected so as to result in formation said graft copolymer having a first backbone incorporating said diluent and said first macromonomer in a first polymer block characterized by a preselected first graft density or a preselected first graft distribution of said first macromonomer. In some embodiments of this aspect, said preselected first graft density is any value selected from the range of 0.05 to 0.75. In some methods, the composition and amount of said diluent is selected to provide both a first preselected first graft density and a first preselected first graft distribution.
Organic Synthesis Applications Of Non-Aqueous Fluoride Salt Solutions
- Pasadena CA, US - Oakland CA, US Christopher M. BATES - Monrovia CA, US Nebojsa MOMCILOVIC - Vienna VA, US Brett M. SAVOIE - Pasadena CA, US Michael A. WEBB - Pasadena CA, US Robert H. GRUBBS - South Pasadena CA, US Jennifer M. MURPHY - Los Angeles CA, US
International Classification:
C07C 209/68
Abstract:
Processes and reaction mixtures including non-aqueous solvent mixtures are presented. Non-aqueous solvent mixtures including fluoride salt and non-aqueous solvent combinations are provided that possess high fluoride ion concentrations useful for a range of applications, including organic synthesis. Further non-aqueous solvent mixtures are provided including a salt possessing a non-fluoride anion and a non-aqueous solvent that, when contacted with aqueous fluoride-containing reagents, extract fluoride ions to form non-aqueous fluoride-ion solutions possessing high fluoride-ion concentrations. The salts include an organic cation that does not possess a carbon in the β-position or does not possess a carbon in the β-position having a bound hydrogen. This salt structure facilitates its ability to be made anhydrous without decomposition. Example anhydrous fluoride salts include (2,2-dimethylpropyl)trimethylammonium fluoride and bis(2,2-dimethylpropyl)dimethylammonium fluoride. The combination of these fluoride salts with at least one fluorine-containing non-aqueous solvent (e.g., bis(2,2,2-trifluoroethyl)ether; (BTFE)) promotes solubility of the salt within the non-aqueous solvents.
Non-Aqueous Fluoride Salts, Solutions, And Their Uses
- Pasadena CA, US - TOKYO, JP Christopher M. BATES - Monrovia CA, US Nebojsa MOMCILOVIC - Vienna VA, US Brett M. SAVOIE - Pasadena CA, US Michael A. WEBB - Pasadena CA, US Robert H. GRUBBS - South Pasadena CA, US Christopher BROOKS - Dublin OH, US Kaoru OMICHI - Columbus OH, US
International Classification:
H01M 10/0568 H01M 10/0569 H01M 10/0525
Abstract:
Electrolyte solutions including at least one anhydrous fluoride salt and at least one non-aqueous solvent are presented. The fluoride salt includes an organic cation having a charge center (e.g., N, P, S, or O) that does not possess a carbon in the β-position or does not possess a carbon in the β-position having a bound hydrogen. This salt structure facilitates its ability to be made anhydrous without decomposition. Example anhydrous fluoride salts include (2,2-dimethylpropyl)trimethylammonium fluoride and bis(2,2-dimethylpropyl)dimethylammonium fluoride. Combining these fluoride salts with at least one fluorine-containing non-aqueous solvent (e.g., bis(2,2,2-trifluoroethyl)ether; (BTFE)) promotes solubility of the salt within the non-aqueous solvents. The solvent may be a mixture of at least one non-aqueous, fluorine-containing solvent and at least one other non-aqueous, fluorine or non-fluorine containing solvent (e.g., BTFE and propionitrile or dimethoxyethane). The electrolyte solutions may be employed in electrochemical cells, such as batteries, fuel cells, electrolysis systems, and capacitors.
Brush Block Copolymer Electrolytes And Electrocatalyst Compositions
- Pasadena CA, US Christopher M. BATES - Monrovia CA, US Alice CHANG - Pasadena CA, US Brendon MCNICHOLAS - Los Angeles CA, US Simon C. JONES - Whittier CA, US
International Classification:
H01M 10/0565 H01M 14/00 H01M 10/0525 C08G 61/02
Abstract:
Provided herein are copolymer electrolytes and electrocatalyst platforms, including brush block copolymers, triblock brush copolymers and pentablock brush copolymers. The copolymers described have beneficial chemical, physical and electrical properties including high ionic conductivity and mechanical strength. In embodiments, for example, the provided copolymer electrolytes and electrocatalyst platforms are doped with lithium salts or mixed with ionic liquids to form ion gels. In some embodiments, the copolymers provided herein self-assemble into physically cross-linked polymer networks with additional useful properties. The provided copolymers have low dispersity in the polymer side chains and do not require post-polymerization modifications.
- Pasadena CA, US Christopher M. BATES - Monrovia CA, US Alice CHANG - Pasadena CA, US Brendon MCNICHOLAS - Los Angeles CA, US Simon C. JONES - Whittier CA, US
International Classification:
C08G 81/00
Abstract:
Provided herein is a class of copolymers, including triblock brush copolymers having specific block configurations, for example, ABC triblock brush copolymers and ABA triblock brush copolymers. In an embodiment, for example, copolymers of the invention incorporate various polymer side chain groups which contribute beneficial physical, chemical, or electronic properties such as increased mechanical or elastic strength, improved ionic or electric conductivity. In some embodiments, the provided copolymers exhibit advantageous steric properties allowing for rapid self-assembly into a variety of morphologies that are substantially different than non-brush, block copolymers.
Film Producer, Line Producer, UPM at Independent Film, Producer, Line Producer, Filmmaker at Maxmedia
Location:
Santa Monica, California
Industry:
Entertainment
Work:
Independent Film - USA, China, Brazil since 2010
Film Producer, Line Producer, UPM
Maxmedia - Santa Monica, CA USA since 2004
Producer, Line Producer, Filmmaker
Skills:
Motion Pictures Film Production Line Producing Production Management China Film Production Brazil Film Production Feature Films Production Managment Film