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6 protocols using 2 chloro 2 propen 1 ol

1

Chromium-Catalyzed Olefin Polymerization

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All reagents were purchased from Sigma-Aldrich: 2,6-pyridinedicarboxylic acid (H2dipic, 99% purity), 2,2′-bypiridine (bipy, 98% purity), 4,4′-dimethoxy-2,2′-bipyridine (dmbipy, 97% purity), chromium trichloride hexahydrate (96%), toluene (99% purity), modified methylaluminoxane (MMAO-12, 7 wt % aluminum in toluene), 2-chloro-2-propen-1-ol (90%).
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2

Synthesis of Pyridine-Chromium Complexes

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The reagents were purchased from Sigma-Aldrich: 2-pyridinecarboxylic acid (2-pic), 99% purity), chromium(III) nitrate hexahydrate (99% purity), lithium carbonate (99% purity), toluene (99% purity), modified methylaluminoxane (MMAO-12, 7 wt% aluminum in toluene), 2-chloro-2-propen-1-ol (90%), and from Stanlab - nitric acid (65%).
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3

Synthesis of Oxovanadium(IV) Microclusters

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The reagents used for the synthesis of oxovanadium(IV) microclusters with 2-phenylpyridine were as follows: vanadyl acetylacetonate (98% purity), oxydiacetic acid (98% purity), and 2-phenylpyridine (98% purity). All reagents were purchased from Sigma-Aldrich (St. Louis, MO, USA).
The olefins 3-buten-2-ol (97% purity), 2-chloro-2-propen-1-ol (90% purity), allyl alcohol (98.5% purity), and 2,3-dibromo-2-propen-1-ol (90% purity) were purchased from Merck, Darmstadt, Germany. The modified methylaluminoxane MMAO-12 (7 wt.%) aluminum in toluene was purchased from Merck.
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4

Synthesis and Characterization of Organometallic Complexes

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All chemical compounds: vanadyl acetylacetonate, 2-phenylpyridine, 4,4′-dimethoxy-2,2′-bipyridine, toluene, dimethylsulfoxide, dipicolinic acid, modified methylaluminoxane (7% aluminum in toluene), 2-propen-1-ol, 2-chloro-2-propen-1-ol, and norbornene were purchased from Merck, Darmstad, Germany. The purity of reagents was in the range 97–100%.
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5

Synthesis and Characterization of Vanadium Complexes

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All chemical compounds: vanadyl acetylacetonate, vanadyl sulfate pentahydrate, 1,10-phenanthroline, thiodiacetate, oxydiacetic acid, 2-phenylpyridine, dipicolinic acid, 4,4′-dimethoxy-2,2′-bipyridine, 2,2′-bipyridine, n-hexane, ethylaluminium dichloride, dimethyl sulfoxide, 3-buten-2-ol, allyl alcohol, 2-chloro-2-propen-1-ol and 2,3-dibromo-2-propen-1-ol were purchased from Merck, Darmstad, Germany. The purity of the reagents was in the range of 97–100%.
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6

Synthesis and Oligomerization of Oxovanadium(IV) Microclusters

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The synthesis procedure of oxovanadium(IV) microclusters with 2-phenylpyridine was as follows:
Mix vanadyl acetylacetonate VO(acac)2 (2.65 g), H2oda (oxydiacetic acid) (1.34 g), and 2.86 mL (0.02 mol) of 2-phenylpyridine, then add 50 mL of water. Boil everything until the solution changes color. The mixture should be refluxed at 100 °C for 2 h. After one month, a new compound was obtained in the form of crystals.
The selected olefins, 3-buten-2-ol, 2-chloro-2-propen-1-ol, allyl alcohol, and 2,3-dibromo-2-propen-1-ol (purchased from Merck), were subjected to oligomerization processes at nitrogen atmosphere, atmospheric pressure, and 65 °C. In the first step, solutions containing 3 µmol of the synthesized complex, 1 mL of toluene, and 1 mL of DMSO were prepared in a glass cell. In the next step, 3 mL of modified methylaluminoxane (MMAO-12, 7 wt.% aluminum in toluene—purchased from Merck) was slowly added into the cell. Next, 1 mL of 3-buten-2-ol, 2-chloro-2-propen-1-ol, allyl alcohol, and 2,3-dibromo-2-propen-1-ol, respectively, were added into the mixture of oxovanadium(IV) microclusters with 2-phenylpyridine activated with modified methylaluminoxane. The solution of each olefin was stirred until a gel was formed.
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