Spin transitions in bis(amidinato)-N-heterocyclic carbene iron(II) and iron(III) complexes.

about

Spin transitions in bis(amidinato)-N-heterocyclic carbene iron(II) and iron(III) complexes.

Item

http://www.wikidata.org/entity/Q53537386

description

2015 nî lūn-bûn

@nan

2015年の論文

@ja

2015年学术文章

@wuu

2015年学术文章

@zh

2015年学术文章

@zh-cn

2015年学术文章

@zh-hans

2015年学术文章

@zh-my

2015年学术文章

@zh-sg

2015年學術文章

@yue

2015年學術文章

@zh-hant

name

Spin transitions in bis

@nl

Spin transitions in bis(amidin ...... n(II) and iron(III) complexes.

@en

type

Item

label

Spin transitions in bis

@nl

Spin transitions in bis(amidin ...... n(II) and iron(III) complexes.

@en

prefLabel

Spin transitions in bis

@nl

Spin transitions in bis(amidin ...... n(II) and iron(III) complexes.

@en

P1476

Spin transitions in bis(amidin ...... n(II) and iron(III) complexes.

@en

P2093

Bo Li

http://www.w3.org/2001/XMLSchema#string

Hilan Z Kaplan

http://www.w3.org/2001/XMLSchema#string

Jeffery A Byers

http://www.w3.org/2001/XMLSchema#string

Jessica L Drake

http://www.w3.org/2001/XMLSchema#string

Matthew J T Wilding

http://www.w3.org/2001/XMLSchema#string

P2860

Iron catalysts for selective anti-Markovnikov alkene hydrosilylation using tertiary silanes.

A mononuclear Fe(III) single molecule magnet with a 3/2↔5/2 spin crossover.

Cytochromes c': biological models for the S = 3/2, 5/2 spin-state admixture?

Preparation and molecular and electronic structures of iron(0) dinitrogen and silane complexes and their application to catalytic hydrogenation and hydrosilation.

A Ru(I) metalloradical that catalyzes nitrene coupling to azoarenes from arylazides.

C-H bond activation of heteroarenes mediated by a half-sandwich iron complex of N-heterocyclic carbene.

Well-defined vanadium organoazide complexes and their conversion to terminal vanadium imides: structural snapshots and evidence for a nitrene capture mechanism.

Bis(imino)pyridine cobalt-catalyzed alkene isomerization-hydroboration: a strategy for remote hydrofunctionalization with terminal selectivity.

P304

16703-16707

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1039/C5DT02440D

http://www.w3.org/2001/XMLSchema#string

P407

English

P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2015-09-14T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P698

26365530

http://www.w3.org/2001/XMLSchema#string