Journal Article
Research Support, Non-U.S. Gov't
Add like
Add dislike
Add to saved papers

Multiple-Hydrogen-Bond Approach to Uncommon Pd(III) Oxidation State: A Pd-Br Chain with High Conductivity and Thermal Stability.

A Br-bridged Pd chain complex with the Pd ion in an uncommon +3 oxidation state, [Pd(dabdOH)2 Br]Br2 (3), was prepared using a new method involving multiple hydrogen bonds. The PdBr chain complex exhibited superior electrical conductivity and thermal stability. An in-plane ligand with an additional hydrogen donor group (hydroxy group), (2S,3S)-2,3-diaminobutane-1,4-diol (dabdOH), was used to create a multiple-hydrogen-bond network, which effectively shrinks the Pd-Br-Pd distance, stabilizing the Pd(III) state up to its decomposition temperature (443 K). 3 shows semiconducting behavior with quite high electrical conductivity (3-38 S cm-1 at room temperature), which is 106 times larger than the previous record for analogous PdBr chains. Indeed, 3 is the most conductive MX-type chain complex reported so far. The precise positional control of ions via a multiple-hydrogen-bond network is a useful method for controlling the electronic states, thermal stability and conductivity of linear coordination polymers.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app