Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging

Research output: Contribution to journalJournal articleResearchpeer-review

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Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging. / Atkins, T.M.; Ganguly, S.; Kauzlarich, S.M.; Cassidy, M.C.; Lee, M.; Marcus, C.M.

In: A C S Nano, Vol. 7, No. 2, 26.02.2013, p. 1609-1617.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Atkins, TM, Ganguly, S, Kauzlarich, SM, Cassidy, MC, Lee, M & Marcus, CM 2013, 'Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging', A C S Nano, vol. 7, no. 2, pp. 1609-1617. https://doi.org/10.1021/nn305462y

APA

Atkins, T. M., Ganguly, S., Kauzlarich, S. M., Cassidy, M. C., Lee, M., & Marcus, C. M. (2013). Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging. A C S Nano, 7(2), 1609-1617. https://doi.org/10.1021/nn305462y

Vancouver

Atkins TM, Ganguly S, Kauzlarich SM, Cassidy MC, Lee M, Marcus CM. Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging. A C S Nano. 2013 Feb 26;7(2):1609-1617. https://doi.org/10.1021/nn305462y

Author

Atkins, T.M. ; Ganguly, S. ; Kauzlarich, S.M. ; Cassidy, M.C. ; Lee, M. ; Marcus, C.M. / Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging. In: A C S Nano. 2013 ; Vol. 7, No. 2. pp. 1609-1617.

Bibtex

@article{027e3f9834e74c558b6f2aeed9e8b8a1,
title = "Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging",
abstract = "We describe the synthesis, materials characterization, and dynamic nuclear polarization (DNP) of amorphous and crystalline silicon nanoparticles for use as hyperpolarized magnetic resonance imaging (MRI) agents. The particles were synthesized by means of a metathesis reaction between sodium silicide (Na Si) and silicon tetrachloride (SiCl) and were surface functionalized with a variety of passivating ligands. The synthesis scheme results in particles of diameter ~10 nm with long size-adjusted Si spin-lattice relaxation (T) times (>600 s), which are retained after hyperpolarization by low-temperature DNP.",
author = "T.M. Atkins and S. Ganguly and S.M. Kauzlarich and M.C. Cassidy and M. Lee and C.M. Marcus",
year = "2013",
month = feb,
day = "26",
doi = "10.1021/nn305462y",
language = "English",
volume = "7",
pages = "1609--1617",
journal = "A C S Nano",
issn = "1936-0851",
publisher = "American Chemical Society",
number = "2",

}

RIS

TY - JOUR

T1 - Synthesis of long T silicon nanoparticles for hyperpolarized Si magnetic resonance imaging

AU - Atkins, T.M.

AU - Ganguly, S.

AU - Kauzlarich, S.M.

AU - Cassidy, M.C.

AU - Lee, M.

AU - Marcus, C.M.

PY - 2013/2/26

Y1 - 2013/2/26

N2 - We describe the synthesis, materials characterization, and dynamic nuclear polarization (DNP) of amorphous and crystalline silicon nanoparticles for use as hyperpolarized magnetic resonance imaging (MRI) agents. The particles were synthesized by means of a metathesis reaction between sodium silicide (Na Si) and silicon tetrachloride (SiCl) and were surface functionalized with a variety of passivating ligands. The synthesis scheme results in particles of diameter ~10 nm with long size-adjusted Si spin-lattice relaxation (T) times (>600 s), which are retained after hyperpolarization by low-temperature DNP.

AB - We describe the synthesis, materials characterization, and dynamic nuclear polarization (DNP) of amorphous and crystalline silicon nanoparticles for use as hyperpolarized magnetic resonance imaging (MRI) agents. The particles were synthesized by means of a metathesis reaction between sodium silicide (Na Si) and silicon tetrachloride (SiCl) and were surface functionalized with a variety of passivating ligands. The synthesis scheme results in particles of diameter ~10 nm with long size-adjusted Si spin-lattice relaxation (T) times (>600 s), which are retained after hyperpolarization by low-temperature DNP.

UR - http://www.scopus.com/inward/record.url?scp=84874433268&partnerID=8YFLogxK

U2 - 10.1021/nn305462y

DO - 10.1021/nn305462y

M3 - Journal article

C2 - 23350651

AN - SCOPUS:84874433268

VL - 7

SP - 1609

EP - 1617

JO - A C S Nano

JF - A C S Nano

SN - 1936-0851

IS - 2

ER -

ID: 45588431