Manganese → gamma-Cyclodextrin Manganese

HRID 1428696

Reaction equation

HRID 1428696 reaction equation
[Mn:1].[CH2:2]([OH:88])[C@H:3]1[O:8][C@@H:7]2[O:9][C@H:10]3[C@H:15]([OH:16])[C@@H:14]([OH:17])[C@@H:13]([O:18][C@H:19]4[C@H:24]([OH:25])[C@@H:23]([OH:26])[C@@H:22]([O:27][C@H:28]5[C@H:33]([OH:34])[C@@H:32]([OH:35])[CH:31]([O:36][CH:37]6[C@H:42]([OH:43])[C@@H:41]([OH:44])[CH:40]([CH:45]7[C@H:50]([OH:51])[C@@H:49]([OH:52])[CH:48]([O:53][C@H:54]8[C@H:59]([OH:60])[C@@H:58]([OH:61])[C@@H:57]([O:62][C@H:63]9[C@H:69]([OH:70])[C@@H:68]([OH:71])[C@@H:66]([O:67][C@H:4]1[C@H:5]([OH:87])[C@H:6]2[OH:86])[O:65][C@@H:64]9[CH2:72][OH:73])[O:56][C@@H:55]8[CH2:74][OH:75])[O:47][C@@H:46]7[CH2:76][OH:77])[O:39][C@@H:38]6[CH2:78][OH:79])[O:30][C@@H:29]5[CH2:80][OH:81])[O:21][C@@H:20]4[CH2:82][OH:83])[O:12][C@@H:11]3[CH2:84][OH:85]>>[CH2:2]([OH:88])[C@H:3]1[O:8][C@@H:7]2[O:9][C@H:10]3[C@H:15]([OH:16])[C@@H:14]([OH:17])[C@@H:13]([O:18][C@H:19]4[C@H:24]([OH:25])[C@@H:23]([OH:26])[C@@H:22]([O:27][C@H:28]5[C@H:33]([OH:34])[C@@H:32]([OH:35])[CH:31]([O:36][CH:37]6[C@H:42]([OH:43])[C@@H:41]([OH:44])[CH:40]([CH:45]7[C@H:50]([OH:51])[C@@H:49]([OH:52])[CH:48]([O:53][C@H:54]8[C@H:59]([OH:60])[C@@H:58]([OH:61])[C@@H:57]([O:62][C@H:63]9[C@H:69]([OH:70])[C@@H:68]([OH:71])[C@@H:66]([O:67][C@H:4]1[C@H:5]([OH:87])[C@H:6]2[OH:86])[O:65][C@@H:64]9[CH2:72][OH:73])[O:56][C@@H:55]8[CH2:74][OH:75])[O:47][C@@H:46]7[CH2:76][OH:77])[O:39][C@@H:38]6[CH2:78][OH:79])[O:30][C@@H:29]5[CH2:80][OH:81])[O:21][C@@H:20]4[CH2:82][OH:83])[O:12][C@@H:11]3[CH2:84][OH:85].[Mn:1]

Participants

3

Reactant 2

HCID 23930Manganese2×HCID 44431027gamma-Cyclodextrine

Product 1

HCID 131732361gamma-Cyclodextrin Manganese

Procedure

23 g of a manganese-based drier, Manganese CEM-ALL® 12% solution (OM Group, Inc.) was added to the above-noted γ-cylodextrin solution. A brown precipitate formed upon addition of the drier. The mixture was stirred for at least 16 hours. The precipitate was filtered off under reduced pressure. The filtrate was light yellow coloured. The precipitate was dried under reduced pressure (around 19 InHg) at 50-60° C. The FTIR spectrum of the resultant inclusion complex is provided in FIG. 1(d).

Workup

  1. customA brown precipitate formed upon addition of the drier
  2. filtrationThe precipitate was filtered off under reduced pressure
  3. dry with materialThe precipitate was dried under reduced pressure (around 19 InHg) at 50-60° C
  4. customThe FTIR spectrum of the resultant inclusion complex is provided in FIG. 1(d)

Sources & evidence

ORD record
ord-be88e115df0e4cc88356a4c07548ff8c
Source dataset
uspto-grants-2015_01
Patent number
US08937119B2

Linked notes

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