Neutron vibrational spectroscopic evidence for short H∙∙∙H contacts in the RNiInH1.4; 1.6 (R = Ce, La) metal hydride

<div>Spectroscopic evidence is presented to show that NADH in aqueous solution does not exist as a folded/unfolded equilibrium but as a single state. The molecule is folded but without base stacking between dihydronicotinamide and adenine.<br></div>

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Secondary cells and batteries containing alkaline or other non-acid electrolytes. Sealed nickel-metal hydride rechargeable single cells

10.3403/01425322u ◽

2015 ◽

Keyword(s):

Metal Hydride ◽

Single Cells ◽

Nickel Metal ◽

Nickel Metal Hydride

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Faculty Opinions recommendation of Spectroscopic evidence for site specific chemistry at a unique iron site of the [4Fe-4S] cluster in ferredoxin:thioredoxin reductase.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1012520.185973 ◽

2003 ◽

Author(s):

Joan Broderick

Keyword(s):

Iron Site ◽

Site Specific ◽

Spectroscopic Evidence ◽

Ferredoxin:Thioredoxin Reductase

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Faculty Opinions recommendation of Crystallographic and spectroscopic evidence for high affinity binding of FeEDTA(H2O)- to the periplasmic nickel transporter NikA.

Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature ◽

10.3410/f.1026940.327492 ◽

2005 ◽

Author(s):

Amy Barrios

Keyword(s):

Affinity Binding ◽

High Affinity Binding ◽

Spectroscopic Evidence ◽

High Affinity

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Metal Hydride Preheater for the M2 Diesel Burner

10.21236/ada361606 ◽

1999 ◽

Author(s):

Joseph Gerstmann ◽

Mark Golben

Keyword(s):

Metal Hydride

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Dihydroflavonol and Flavonol Derivatives from Macaranga Recurvata

Natural Product Communications ◽

10.1177/1934578x1200701013 ◽

2012 ◽

Vol 7 (10) ◽

pp. 1934578X1200701

Author(s):

Mulyadi Tanjung ◽

Euis H. Hakim ◽

Elfahmi ◽

Jalifah Latip ◽

Yana M. Syah

Keyword(s):

Strong Activity ◽

Spectroscopic Evidence ◽

New Compounds ◽

Flavonol Derivatives

Two new dihydroflavonol derivatives, macarecurvatins A and B, have been isolated from the leaves of Macaranga recurvata(Euphorbiaceaae), along with the known compounds diisoprenylaromadendrin, glyasperin A and broussoflavonol F. The structures of the new compounds were determined on the basis of spectroscopic evidence. Upon cytotoxic evaluation against P-388 cells, macarecurvatin B showed strong activity with an IC50 of 0.83 μM.

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