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序号	专利名	申请号	申请日	公开（公告）号	公开（公告）日	发明人
41	Process for the arylation of aromatic compounds	US15012061	1961-11-06	US3231629A	1966-01-25	BRYSON MCCALL ERNEST; JAMES ROBERTS RYLAND

42	Dimerization of styrene and vinyl pyridines in the presence of atomic hydrogen	US6642460	1960-11-01	US3192218A	1965-06-29	SOLOMON PAUL W

43	Process for producing aromatic compounds by pyrolysis	US78094358	1958-12-17	US3080434A	1963-03-05	ODIOSO RAYMOND C; FRECH KENNETH J

44	Preparation of hydrocarbons	US70276557	1957-12-16	US2956086A	1960-10-11	FRANK CHARLES E; LEEBRICK JOHN R

45	ALKYLATION PROCESSES USING LIQUID LEWIS ACID CATALYSTS	US15867445	2018-01-10	US20180127335A1	2018-05-10	Erin M. Broderick; Alakananda Bhattacharyya; Peter K. Coughlin
An alkylation process is described. The alkylation process includes contacting a feed comprising a paraffin or an aromatic with an olefin feed in the presence of a liquid Lewis acid catalyst in an alkylation reaction zone under alkylation conditions to form a reaction mixture comprising alkylation products and the liquid Lewis acid catalyst. The liquid Lewis acid catalyst is the liquid reaction product of a donor molecule and a metal halide. The alkylation products are separated from the liquid Lewis acid catalyst and recovered.
46	Tandem transfer hydrogenation and oligomerization for hydrocarbon production	US15596255	2017-05-16	US09944572B2	2018-04-17	David Leitch; Jay A. Labinger; John E. Bercaw; Yan Choi Lam
A method for coupling an alkane with an alkene using a hydrogen transfer catalyst and an alkene dimerization catalyst to form one or more higher molecular weight hydrocarbons.
47	TANDEM TRANSFER HYDROGENATION AND OLIGOMERIZATION FOR HYDROCARBON PRODUCTION	US14157744	2014-01-17	US20140200376A1	2014-07-17	David Leitch; Jay A. Labinger; John E. Bercaw; Yan Choi Lam
The disclosure provides for hydrocarbon production by hydrogenation and oligomerizaton and, more particularly, to catalysis of alkanes and alkenes by a tandem transfer hydrogenation and oligomerization.
48	Toluene and styrene derived telomer distributions and brominated flame retardants produced therefrom	US13130098	2009-11-30	US08648140B2	2014-02-11	William J. Layman, Jr.; Charles H. Kolich; Arthur G. Mack; Steven A. Anderson; Jonathan P. McCarney; Junzuo Wang
This invention relates to novel and useful toluene and styrene derived telomer distributions, such distributions being desirable substrates for the preparation of brominated flame retardants.
49	COMPOUNDS FOR NEUTRON RADIATION DETECTORS AND SYSTEMS THEREOF	US12418450	2009-04-03	US20100256923A1	2010-10-07	Stephen A. Payne; Wolfgang Stoeffl; Natalia P. Zaitseva; Nerine J. Cherepy; M. Leslie Carman
One embodiment includes a material exhibiting an optical response signature for neutrons that is different than an optical response signature for gamma rays, said material exhibiting performance comparable to or superior to stilbene in terms of distinguishing neutrons from gamma rays, wherein the material is not stilbene. Another embodiment includes a substantially pure crystal exhibiting an optical response signature for neutrons that is different than an optical response signature for gamma rays, the substantially pure crystal comprising a material selected from a group consisting of: 1-1-4-4-tetraphenyl-1-3-butadiene; 2-fluorobiphenyl-4-carboxylic acid; 4-biphenylcarboxylic acid; 9-10-diphenylanthracene; 9-phenylanthracene; 1-3-5-triphenylbenzene; m-terphenyl; bis-MSB; p-terphenyl; diphenylacetylene; 2-5-diphenyoxazole; 4-benzylbiphenyl; biphenyl; 4-methoxybiphenyl; n-phenylanthranilic acid; and 1-4-diphenyl-1-3-butadiene.
50	Fluids Having Partially Hydrogenated Substituted Styrene Linear Dimers and Method of Making Same	US12607758	2009-10-28	US20100048434A1	2010-02-25	Mark Paul Hagemeister; Thomas R. Forbus, JR.
A basestock that comprises a fully hydrogenated substituted styrene linear dimer; a partially hydrogenated mono-aromatic substituted styrene linear dimer; and a partially hydrogenated di-aromatic substituted styrene linear dimer. A process of producing a basestock that comprises reacting a feed stream that comprises substituted styrene, alcohol, and a dimerization catalyst, in the presence of a solvent, to form a crude slurry of dimerized substituted styrene; and partially hydrogenating the dimerized substituted styrene with hydrogen over a Group VIII catalyst to form a basestock that comprises a fully hydrogenated substituted styrene linear dimer and a partially hydrogenated substituted styrene linear dimer.
51	Aryl-substituted acyclic enediyne compounds	US10847667	2004-05-18	US07332623B2	2008-02-19	Ming-Jung Wu; Chi-Fong Lin
This invention provides aryl-substituted acyclic enediyne compounds of formula (I): or a pharmaceutically acceptable salt or solvate thereof, wherein R1=R2=H; or R1 and R2 together form a moiety represented by the formula R3 represents a substituted or unsubstituted alkyl having 4-30 carbon atoms, or a substituted or unsubstituted aryl group having 3-30 carbon atoms; and R4 represents a substituted or unsubstituted aryl group having 3-30 carbon atoms; with the proviso that R3 is not butyl, pentyl, tetrahydropyranyloxymethyl, tetrahydropyranyloxypropyl or phenyl when R1=R2=H and R4 is o-cyanophenyl,; and with the proviso that R3 is not butyl when R1=R2=H and R4 is phenyl. The compounds of formula (I) are found to have inhibitory activities against topoisomerase I or act as a S phase or G2/M phase blocker.
52	Method of reacting carboxylic acids	US10659738	2003-09-11	US07279082B2	2007-10-09	Paul Watts; Stephen John Haswell
A carboxylic acid molecule (R COOH) is subjected to an electric field in a micro-reactor. The molecule decarboxyles to form a radical (R•). Two radicals (R•) can dimerise to form the product (R—R). It is believed that the reaction occurs away from the electrodes used to apply the electric field (but may also occur at the electrode surfaces).
53	P-chiral phospholanes and phosphocyclic compounds and their use in asymmetric catalytic reactions	US11031159	2005-01-07	US20050119495A1	2005-06-02	Xumu Zhang; Wenjun Tang
Chiral ligands and metal complexes based on such chiral ligands useful in asymmetric catalysis are disclosed. The metal complexes according to the present invention are useful as catalysts in asymmetric reactions, such as, hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition; epoxidation, kinetic resolution and [m+n] cycloaddition. Processes for the preparation of the ligands are also described.
54	P-chiral phospholanes and phosphocyclic compounds and their use in asymmetric catalytic reactions	US10856014	2004-05-28	US20040229846A1	2004-11-18	Xumu Zhang; Wenjun Tang
Chiral ligands and metal complexes based on such chiral ligands useful in asymmetric catalysis are disclosed. The metal complexes according to the present invention are useful as catalysts in asymmetric reactions, such as, hydrogenation, hydride transfer, allylic alkylation, hydrosilylation, hydroboration, hydrovinylation, hydroformylation, olefin metathesis, hydrocarboxylation, isomerization, cyclopropanation, Diels-Alder reaction, Heck reaction, isomerization, Aldol reaction, Michael addition; epoxidation, kinetic resolution and nullmnullnnull cycloaddition. Processes for the preparation of the ligands are also described.
55	Acid catalyzed isomerization of substituted diaryls	US09531248	2000-03-21	US06433236B1	2002-08-13	David Anthony Schiraldi; Alexei Viktorovich Iretski; Sheldon Christopher Sherman; Laren Malcolm Tolbert; Mark Gilmore White
A substituted diaryl compound or a mixture of substituted diaryl compounds, such as dimethylbiaryl compounds are isomerized by treatment with a strong acid or mixtures of strong acids in the absence of any additional catalyst. The strong acid or mixture of acids has a Hammett acidity of less than about −12.6. The isomerization reaction conditions such as reaction temperature, amount of acid, and amount of solvent can be adjusted to selectively produce desired isomers in high yields. One or more desired isomers may be produced in high yields by isomerization of substituted diaryl compounds and selectively removing one or more desired isomers from the resulting equilibrium mixture of isomers. The isomer mixture may be re-isomerized subsequent to selective removal of the desired isomer to produce additional amounts of desired isomer. The isomerization may be employed to substantially reduce the amount of at least one isomer substituted in the 2-position or to substantially increase the amount of at least one isomer substituted in at least the 3-position, the 4-position or the 4-position for the production of at least substantially linear or crystalline polymers.
56	Polymers made from unsaturated monomers and polar substituted saturated monomers	US82286769	1969-05-05	US3803110A	1974-04-09	RICHARDS D; WILLIAMS R; SCILLY N; WILLIAMS F
ALKENES ARE REACTED WITH ELECTRON DONORS IN THE PRESENCE OF COMONOMERS HAVING FUBCTIONAL GROUPS SUCEPTIBLE TO NUCLEOPHILIC ATTACK SUCH AS HALIDE OR EPOXY GROUPS. THE USE OF COMOMOMERS HAVING ONE FUNCTIONAL GROUP PRODUCES COMONOMER-TEMPERATURED ALKENE OILGOMERS WHILST THE USE OF COMONOMERS HAVING AT LEAST TWO FUNCTIONAL GROUPS PRODUCES COPOLYMERS.
57	Synthetic power transmission fluids	US3577361D	1968-05-22	US3577361A	1971-05-04	HAMMANN WILLIAM C; SCHISLA ROBERT M
AN IMPROVED METHOD OF TRANSMITTING POWER IN HYDRAULICALLY-OPERATED MECHANISMS WHICH COMPRISES USING AS THE OPERATIVE FLUID CERTAIN TETRAALYKYL SUBSTITUTED ALKYLENE-LINKED DICYCLOHEXYL COMPOUNDS.
58	Conversion of diphenylalkane to higher value products	US56171866	1966-06-30	US3401208A	1968-09-10	KERFOOT OLIVER C; KREHBIEL DELMAR D

59	Lubricating oil compositions containing viscosity index improving agents	US3394660	1960-06-06	US3057801A	1962-10-09	WILGUS DONOVAN R

60	Chemical separation and purification of diarylbutanes	US86035059	1959-12-18	US3013092A	1961-12-12	WATSON LLOYD M; ALLGEIER EDWIN A

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