Multiple Aromatic C–H Bond Activations by an
Unsaturated Dirhenium Carbonyl Complex
Version 2 2019-01-11, 19:34
Version 1 2019-01-11, 19:34
Posted on 2019-01-11 - 19:34
Reactions
of Re2(CO)8(μ-C6H5)(μ-H), 1, with naphthalene and anthracene
have yielded the first multiply-CH activated arene products through
the reductive elimination of benzene from 1 and multiple
oxidative-additions of the dirhenium octacarbonyl grouping to these
polycyclic aromatic compounds under very mild conditions. In addition,
compound 1 was found to react with itself to yield the
bis-Re2-metalated C6H4 bridged compound
Re2(CO)8(μ-H)(μ-1,μ-3-C6H4)Re2(CO)8(μ-H), 3. Reaction of 1 with naphthalene yielded two
doubly CH activated isomers, Re2(CO)8(μ-H)(μ–η2-1,2-μ–η2-3,4-C10H6)Re2(CO)8(μ-H), 4, 41% yield, and Re2(CO)8(μ-H)(μ–η2-1,2-μ–η2-5,6-C10H6)Re2(CO)8(μ-H), 5, via the mono CH activated intermediate Re2(CO)8(μ–η2-C10H7)(μ-H), 2. Compound 4 contains two Re2(CO)8(μ-H) groups on one C6 ring formed by CH
activations at the 2- and 4-positions. Compound 5 contains
two Re2(CO)8(μ-H) groups; one formed by
CH activation at the 2-position on one C6 ring and the
other formed by CH activation at the 6-position (or centrosymmetrically
related 2′-position) on the second C6 ring. The
Re2(CO)8(μ-H) groups are coordinated to
the C6 rings by binuclear σ + π coordination
to two adjacent carbon atoms in the rings. Compound 1 reacts with anthracene to yield the mono-CH activated compound Re2(CO)8(μ–η2-1,2-C14H9)(μ-H), 6, and two doubly
CH activated compounds, Re2(CO)8(μ-H)(μ–η2-1,2-μ–η2-3,4-C14H8)Re2(CO)8(μ-H), 7, and Re2(CO)8(μ-H)(μ–η2-1,2-μ–η2-5,6-C14H8)Re2(CO)8(μ-H), 8. Compounds 7 and 8 are isomers that are
structurally similar to 4 and 5. Compounds 7 and 8 can also be obtained in good yields from
the reaction of 6 with 1. In the presence
of a 5/1 ratio of 1/anthracene, a small amount (5% yield)
of the tetra-substituted anthracene product [Re2(CO)8(μ-H)]4(μ–η2-1,2-μ–η2-3,4-μ–η2-5,6-μ–η2-7,8-C14H6), 9, was formed. Compound 9 contains four σ + π coordinated Re2(CO)8(μ-H) groups formed by oxidative additions of the CH
bonds of anthracene to the Re2(CO)8 groups at
the 2, 4, 6, and 8 positions of the three ring system. Molecular orbital
calculations have been performed for all new compounds in order to
develop an understanding of the bonding of the ring systems to the
Re2(CO)8(μ-H) groups. All new compounds
were characterized by single-crystal X-ray diffraction analyses.
CITE THIS COLLECTION
DataCite
3 Biotech
3D Printing in Medicine
3D Research
3D-Printed Materials and Systems
4OR
AAPG Bulletin
AAPS Open
AAPS PharmSciTech
Abhandlungen aus dem Mathematischen Seminar der Universität Hamburg
ABI Technik (German)
Academic Medicine
Academic Pediatrics
Academic Psychiatry
Academic Questions
Academy of Management Discoveries
Academy of Management Journal
Academy of Management Learning and Education
Academy of Management Perspectives
Academy of Management Proceedings
Academy of Management Review
Adams, Richard D.; Dhull, Poonam; Smith, Mark D.; Tedder, Jonathan D. (2019). Multiple Aromatic C–H Bond Activations by an
Unsaturated Dirhenium Carbonyl Complex. ACS Publications. Collection. https://doi.org/10.1021/acs.inorgchem.8b03201
or
Select your citation style and then place your mouse over the citation text to select it.
SHARE
Usage metrics
Read the peer-reviewed publication
AUTHORS (4)
RA
Richard D. Adams
PD
Poonam Dhull
MS
Mark D. Smith
JT
Jonathan D. Tedder