Muhammad S. Khan

Dr. Muhammad S. Khan

Department of Chemistry, Sultan Qaboos University, Al-Khod 123, Oman
orcid

Research Focus & Metrics

Academic Career Length

43Years (1984-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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24 August 2001 in Journal of the American Chemical Society
Verified
Journal Article
Closed access
JWJoanne S. Wilson
Joanne S. Wilson
NCNazia Chawdhury
Nazia Chawdhury
MAMuna R. A. Al-Mandhary
Muna R. A. Al-Mandhary
MYM. Younus
M. Younus
Muhammad S. KhanMuhammad S. Khan
Muhammad S. Khan
RFRichard H. Friend
Richard H. Friend

1 October 2001 in Nature
Verified
Journal Article
Closed access
JWJ. S. Wilson
J. S. Wilson
ADA. S. Dhoot
A. S. Dhoot
ASA. J. A. B. Seeley
A. J. A. B. Seeley
Muhammad S. KhanMuhammad S. Khan
Muhammad S. Khan
AKA. Köhler
A. Köhler
RFR. H. Friend
R. H. Friend

10 November 2005 in Physical Review B
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Journal Article
Closed access
PDF file
ÖMÖ. Mermer
Ö. Mermer
GVG. Veeraraghavan
G. Veeraraghavan
TFT. L. Francis
T. L. Francis
YSY. Sheng
Y. Sheng
DND. T. Nguyen
D. T. Nguyen
Muhammad S. KhanMuhammad S. Khan
Muhammad S. Khan
Following the recent observation of large magnetoresistance at room temperature in polyfluorene sandwich devices, we have performed a comprehensive magnetoresistance study on a set of organic semiconductor sandwich devices made from different π-conjugated polymers and small molecules. The study includes a range of materials that show greatly different chemical structure, mobility, and spin-orbit coupling strength. We study both hole and electron transporters at temperatures ranging from 10 K to 300 K. We observe large negative or positive magnetoresistance (up to 10% at 300 K and 10 mT) depending on material and device operating conditions. We discuss our results in the framework of known magnetoresistance mechanisms and find that none of the existing models can explain our results.

3 January 2023 in Chemical Society Reviews
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Journal Article
Open access
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AHAshanul Haque
Ashanul Haque
KAKhalaf M. Alenezi
Khalaf M. Alenezi
Muhammad S. KhanMuhammad S. Khan
Muhammad S. Khan
Wai-yeung WongWai-yeung Wong
Wai-yeung Wong
Paul Robert RaithbyPaul Robert Raithby
Paul Robert Raithby
The design and development of functional materials with real-life applications are highly demanding. Understanding and controlling inter- and intra-molecular interactions provide opportunities to design new materials. A judicious manipulation of the molecular structure significantly alters such interactions and can boost selected properties and functions of the material. There is burgeoning evidence of the beneficial effects of non-covalent interactions (NCIs), showing that manipulating NCIs may generate functional materials with a wide variety of physical properties leading to applications in catalysis, drug delivery, crystal engineering, etc. This prompted us to review the implications of NCIs on the molecular packing, optical properties, and applications of functional π-conjugated materials. To this end, this tutorial review will cover different types of interactions (electrostatic, π-interactions, metallophilic, etc.) and their impact on π-conjugated materials. Attempts have also been made to delineate the effects of weak interactions on opto-electronic (O-E) applications.

25 February 1999 in The Journal of Chemical Physics
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Journal Article
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NCN. Chawdhury
N. Chawdhury
AKA. Köhler
A. Köhler
RFR. H. Friend
R. H. Friend
Wai-yeung WongWai-yeung Wong
Wai-yeung Wong
JLJ. Lewis
J. Lewis
Muhammad S. KhanMuhammad S. Khan
Muhammad S. Khan
Soluble, rigid-rod organometallic polymers trans-[-Pt(PBu3n)2–C≡C–R–C≡C–]∞ (R=bithienyl 2, terthienyl 3) have been synthesized in good yields by the CuI-catalyzed dehydrohalogenation reaction of trans-[Pt(PBu3n)2Cl2] with one equivalent of the diterminal alkynyl oligothiophenes H–C≡C–R–C≡C–H in CH2Cl2/iPr2NH at room temperature. We report the thermal properties, and the optical absorption, photoluminescence, and photocurrent action spectra of 1 (trans-[–Pt(PBu3n)2–C≡C–R–C≡C–]∞, R=thienyl ), 2 and 3 as a function of the number of thiophene rings within the bridging ligand. With increasing thiophene content, the optical gap is reduced and the vibronic structure of the singlet emission changes toward that typical for oligothiophenes. We also find the intersystem crossing from the singlet excited state to the triplet excited state to become reduced, while the singlet–triplet energy gap remains unaltered. The latter implies that, in these systems, the T1 triplet excited state is extended over several thiophene rings. The photoconducting properties do not depend on the size of the thiophene fragment. We discuss and compare our results with studies on oligothiophenes and related organometallic polymers.

1 April 2017 in Bioorganic & Medicinal Chemistry
Verified
Journal Article
Closed access
AHAshanul Haque
Ashanul Haque
MFMd Serajul Haque Faizi
Md Serajul Haque Faizi
JRJahangir Ahmad Rather
Jahangir Ahmad Rather
Muhammad S. KhanMuhammad S. Khan
Muhammad S. Khan