Iridium containing hydrosilylation catalysts and compositions containing the catalysts
US-9221041-B2 · Dec 29, 2015 · US
US10759819B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10759819-B2 |
| Application number | US-201916412768-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 15, 2019 |
| Priority date | May 15, 2018 |
| Publication date | Sep 1, 2020 |
| Grant date | Sep 1, 2020 |
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The present disclosure provides a single-side modified β-Anderson-type heteropolymolybdate organic derivative having an anionic moiety with a general formula represented by: β-{[RC(CH 2 O) 3 ]M(OH) 3 Mo 6 O 18 } 3− ; β represents a non-planar folded structure; R=substituted or unsubstituted phenyl, C n H 2n X (n is an integer from 0 to 22; X═H, OH, NH(CH 2 ) 3 SO 3 H, NHCH 2 COOH, NH 2 , or NO 2 ); M=Cr 3+ . The single-side modified β-Anderson-type heteropolymolybdate organic derivative can be prepared under hydrothermal conditions.
Opening claim text (preview).
What is claimed is: 1. A single-side modified β-Anderson-type heteropolymolybdate organic derivative comprising an anionic moiety and a cationic moiety, wherein the anionic moiety has a general formula represented by: β-{[RC(CH 2 O) 3 ]M(OH) 3 Mo 6 O 18 } 3− , wherein: β represents a non-planar folded structure; R=substituted or unsubstituted phenyl, C 1 H 2n X (n is an integer from 0 to 22; X═H, OH, NH(CH 2 ) 3 SO 3 H, NHCH 2 COOH, NH 2 , or NO 2 ); and M=Cr 3+ . 2. The single-side modified β-Anderson-type heteropolymolybdate organic derivative according to claim 1 , wherein the cation of the cationic moiety comprises one or more of TBA + , TEA + , TMA + , NH 4 + , and H 3 NC(CH 2 O) 3 ±. 3. The single-side modified β-Anderson-type heteropolymolybdate organic derivative according to claim 1 , wherein the single-side modified β-Anderson-type heteropolymolybdate organic derivative includes: (NH 4 ) 3 .β-{[O 3 S(CH 2 ) 3 NH 2 C(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }; (NH 4 ) 3 .β-{[C 2 H 5 C(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }; (NH 4 ) 3 .β-{[C 6 H 5 C(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }; (NH 4 ) 3 .β-{[HOOCCH 2 NHC(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }; [H 3 NC(CH 2 O) 3 ] 2 .β-{[H 3 NC(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }; [TBA] 4 .β-{[H 2 NC(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }Br; [TBA] 3 .β-{[CH 3 C(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }; (NH 4 ) [TBA] 4 .β-{[C 2 H 5 C(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 } Br 2 ; [TEA] [TBA] 3 .β-{[HOCH 2 C(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }Cl; or [TMA] 2 .β-{[H 3 NC(CH 2 O) 3 ]CrMo 6 O 18 (OH) 3 }.
compounds without a metal-carbon linkage · CPC title
containing metals, e.g. organo-metallic compounds, coordination complexes · CPC title
to carbon atoms of acyclic carbon skeletons · CPC title
with one amino group and at least two hydroxy groups bound to the carbon skeleton · CPC title
containing amino groups bound to the carbon skeleton · CPC title
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