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Paralia (Bacillariophyta) stowaways in ship ballast: implications for biogeography and diversity of the genus.

Journal of biological research (Thessalonike, Greece)

MacGillivary ML, Kaczmarska I.
PMID: 25984507
J Biol Res (Thessalon). 2015 Feb 15;22(1):2. doi: 10.1186/s40709-015-0024-5. eCollection 2015 Dec.

BACKGROUND: The genus Paralia Heiberg is one of the most recognizable, widely distributed and commonly reported diatoms from contemporary coastal marine environments and ship ballast. Species discovery has historically been made in diatoms through the recognition of morphological discontinuities...

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MacGillivary ML, Kaczmarska I. Paralia (Bacillariophyta) stowaways in ship ballast: implications for biogeography and diversity of the genus. J Biol Res (Thessalon). 2015;22(1):2doi: 10.1186/s40709-015-0024-5.
MacGillivary, M. L., & Kaczmarska, I. (2015). Paralia (Bacillariophyta) stowaways in ship ballast: implications for biogeography and diversity of the genus. Journal of biological research (Thessalonike, Greece), 22(1), 2. https://doi.org/10.1186/s40709-015-0024-5
MacGillivary, Michael L, and Kaczmarska, Irena. "Paralia (Bacillariophyta) stowaways in ship ballast: implications for biogeography and diversity of the genus." Journal of biological research (Thessalonike, Greece) vol. 22,1 (2015): 2. doi: https://doi.org/10.1186/s40709-015-0024-5
MacGillivary ML, Kaczmarska I. Paralia (Bacillariophyta) stowaways in ship ballast: implications for biogeography and diversity of the genus. J Biol Res (Thessalon). 2015 Feb 15;22(1):2. doi: 10.1186/s40709-015-0024-5. eCollection 2015 Dec. PMID: 25984507; PMCID: PMC4389653.
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Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability.

Journal of the American Chemical Society

Rupasinghe TP, Hutchins KM, Bandaranayake BS, Ghorai S, Karunatilake C, Bučar DK, Swenson DC, Arnold MA, MacGillivray LR, Tivanski AV.
PMID: 26407029
J Am Chem Soc. 2015 Oct 14;137(40):12768-71. doi: 10.1021/jacs.5b07873. Epub 2015 Oct 02.

A correlation between Young's modulus, as determined by using nanoindentation atomic force microscopy (AFM), and atomic polarizability is observed for members of a series of cocrystals based on systematic changes to one cocrystal component. Time domain spectroscopy over terahertz...

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Rupasinghe TP, Hutchins KM, Bandaranayake BS, et al. Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability. J Am Chem Soc. 2015;137(40):12768-71doi: 10.1021/jacs.5b07873.
Rupasinghe, T. P., Hutchins, K. M., Bandaranayake, B. S., Ghorai, S., Karunatilake, C., Bučar, D. K., Swenson, D. C., Arnold, M. A., MacGillivray, L. R., & Tivanski, A. V. (2015). Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability. Journal of the American Chemical Society, 137(40), 12768-71. https://doi.org/10.1021/jacs.5b07873
Rupasinghe, Thilini P, et al. "Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability." Journal of the American Chemical Society vol. 137,40 (2015): 12768-71. doi: https://doi.org/10.1021/jacs.5b07873
Rupasinghe TP, Hutchins KM, Bandaranayake BS, Ghorai S, Karunatilake C, Bučar DK, Swenson DC, Arnold MA, MacGillivray LR, Tivanski AV. Mechanical Properties of a Series of Macro- and Nanodimensional Organic Cocrystals Correlate with Atomic Polarizability. J Am Chem Soc. 2015 Oct 14;137(40):12768-71. doi: 10.1021/jacs.5b07873. Epub 2015 Oct 02. PMID: 26407029.
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Halogen-Bond-Templated [2+2] Photodimerization in the Solid State: Directed Synthesis and Rare Self-Inclusion of a Halogenated Product.

Angewandte Chemie (International ed. in English)

Sinnwell MA, MacGillivray LR.
PMID: 26836572
Angew Chem Int Ed Engl. 2016 Mar 01;55(10):3477-80. doi: 10.1002/anie.201510912. Epub 2016 Feb 02.

A ditopic halogen-bond acceptor organizes a diiodooctafluorostilbene for a [2+2] photodimerization reaction to take place between two stilbene molecules in the solid state. The resultant cyclobutane product is functionalized with halogen atoms and undergoes self-assembly to form a channel-type...

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Sinnwell MA, MacGillivray LR. Halogen-Bond-Templated [2+2] Photodimerization in the Solid State: Directed Synthesis and Rare Self-Inclusion of a Halogenated Product. Angew Chem Int Ed Engl. 2016;55(10):3477-80doi: 10.1002/anie.201510912.
Sinnwell, M. A., & MacGillivray, L. R. (2016). Halogen-Bond-Templated [2+2] Photodimerization in the Solid State: Directed Synthesis and Rare Self-Inclusion of a Halogenated Product. Angewandte Chemie (International ed. in English), 55(10), 3477-80. https://doi.org/10.1002/anie.201510912
Sinnwell, Michael A, and MacGillivray, Leonard R. "Halogen-Bond-Templated [2+2] Photodimerization in the Solid State: Directed Synthesis and Rare Self-Inclusion of a Halogenated Product." Angewandte Chemie (International ed. in English) vol. 55,10 (2016): 3477-80. doi: https://doi.org/10.1002/anie.201510912
Sinnwell MA, MacGillivray LR. Halogen-Bond-Templated [2+2] Photodimerization in the Solid State: Directed Synthesis and Rare Self-Inclusion of a Halogenated Product. Angew Chem Int Ed Engl. 2016 Mar 01;55(10):3477-80. doi: 10.1002/anie.201510912. Epub 2016 Feb 02. PMID: 26836572.
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'Template-switching': a supramolecular strategy for the quantitative, gram-scale construction of a molecular target in the solid state.

Chemical communications (Cambridge, England)

Friscic T, MacGillivray LR.
PMID: 12809243
Chem Commun (Camb). 2003 Jun 07;(11):1306-7.

A template-switching strategy based on the modularity of template-directed solid-state synthesis has been successfully utilised to achieve a quantitative, stereospecific solid-state synthesis of a p-[2.2]-cyclophane target in gram quantities.

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Friscic T, MacGillivray LR. 'Template-switching': a supramolecular strategy for the quantitative, gram-scale construction of a molecular target in the solid state. Chem Commun (Camb). 2003;(11):1306-7
Friscic, T., & MacGillivray, L. R. (2003). 'Template-switching': a supramolecular strategy for the quantitative, gram-scale construction of a molecular target in the solid state. Chemical communications (Cambridge, England), (11), 1306-7.
Friscic, Tomislav, and MacGillivray, Leonard R. "'Template-switching': a supramolecular strategy for the quantitative, gram-scale construction of a molecular target in the solid state." Chemical communications (Cambridge, England) vol. ,11 (2003): 1306-7.
Friscic T, MacGillivray LR. 'Template-switching': a supramolecular strategy for the quantitative, gram-scale construction of a molecular target in the solid state. Chem Commun (Camb). 2003 Jun 07;(11):1306-7. PMID: 12809243.
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Soluble Solids Content of Different Regions of Watermelons.

Plant physiology

Macgillivray JH.
PMID: 16654134
Plant Physiol. 1947 Oct;22(4):637-40. doi: 10.1104/pp.22.4.637.

No abstract available.

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Macgillivray JH. Soluble Solids Content of Different Regions of Watermelons. Plant Physiol. 1947;22(4):637-40doi: 10.1104/pp.22.4.637.
Macgillivray, J. H. (1947). Soluble Solids Content of Different Regions of Watermelons. Plant physiology, 22(4), 637-40. https://doi.org/10.1104/pp.22.4.637
Macgillivray, J H. "Soluble Solids Content of Different Regions of Watermelons." Plant physiology vol. 22,4 (1947): 637-40. doi: https://doi.org/10.1104/pp.22.4.637
Macgillivray JH. Soluble Solids Content of Different Regions of Watermelons. Plant Physiol. 1947 Oct;22(4):637-40. doi: 10.1104/pp.22.4.637. PMID: 16654134; PMCID: PMC405905.
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Removal of metal ions from aqueous solutions using chelating task-specific ionic liquids.

Dalton transactions (Cambridge, England : 2003)

Harjani JR, Friscić T, MacGillivray LR, Singer RD.
PMID: 19024358
Dalton Trans. 2008 Sep 14;(34):4595-601. doi: 10.1039/b806369a.

A new class of imidazolium salts with appended aminodiacetic acid moieties as di-tert-butyl esters has been synthesized. An improved synthetic route compared to that previously reported is described. These task specific ionic liquids have been used for the formation...

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Harjani JR, Friscić T, MacGillivray LR, et al. Removal of metal ions from aqueous solutions using chelating task-specific ionic liquids. Dalton Trans. 2008;(34):4595-601doi: 10.1039/b806369a.
Harjani, J. R., Friscić, T., MacGillivray, L. R., & Singer, R. D. (2008). Removal of metal ions from aqueous solutions using chelating task-specific ionic liquids. Dalton transactions (Cambridge, England : 2003), (34), 4595-601. https://doi.org/10.1039/b806369a
Harjani, Jitendra R, et al. "Removal of metal ions from aqueous solutions using chelating task-specific ionic liquids." Dalton transactions (Cambridge, England : 2003) vol. ,34 (2008): 4595-601. doi: https://doi.org/10.1039/b806369a
Harjani JR, Friscić T, MacGillivray LR, Singer RD. Removal of metal ions from aqueous solutions using chelating task-specific ionic liquids. Dalton Trans. 2008 Sep 14;(34):4595-601. doi: 10.1039/b806369a. PMID: 19024358.
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Coordination-driven self-assembly directs a single-crystal-to-single-crystal transformation that exhibits photocontrolled fluorescence.

Journal of the American Chemical Society

Papaefstathiou GS, Zhong Z, Geng L, MacGillivray LR.
PMID: 15281786
J Am Chem Soc. 2004 Aug 04;126(30):9158-9. doi: 10.1021/ja047819n.

Coordination-driven self-assembly is employed to direct a single-crystal-to-single-crystal [2 + 2] photodimerization that exhibits tunable fluorescence.

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Papaefstathiou GS, Zhong Z, Geng L, et al. Coordination-driven self-assembly directs a single-crystal-to-single-crystal transformation that exhibits photocontrolled fluorescence. J Am Chem Soc. 2004;126(30):9158-9doi: 10.1021/ja047819n.
Papaefstathiou, G. S., Zhong, Z., Geng, L., & MacGillivray, L. R. (2004). Coordination-driven self-assembly directs a single-crystal-to-single-crystal transformation that exhibits photocontrolled fluorescence. Journal of the American Chemical Society, 126(30), 9158-9. https://doi.org/10.1021/ja047819n
Papaefstathiou, Giannis S, et al. "Coordination-driven self-assembly directs a single-crystal-to-single-crystal transformation that exhibits photocontrolled fluorescence." Journal of the American Chemical Society vol. 126,30 (2004): 9158-9. doi: https://doi.org/10.1021/ja047819n
Papaefstathiou GS, Zhong Z, Geng L, MacGillivray LR. Coordination-driven self-assembly directs a single-crystal-to-single-crystal transformation that exhibits photocontrolled fluorescence. J Am Chem Soc. 2004 Aug 04;126(30):9158-9. doi: 10.1021/ja047819n. PMID: 15281786.
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Traumatic bilateral knee dislocations, unilateral hip dislocation, and contralateral humeral amputation: a case report.

HSS journal : the musculoskeletal journal of Hospital for Special Surgery

Voos JE, Heyworth BE, Piasecki DP, Henn RF, MacGillivray JD.
PMID: 19052715
HSS J. 2009 Feb;5(1):40-4. doi: 10.1007/s11420-008-9100-9. Epub 2008 Dec 04.

Bilateral traumatic knee dislocations are a rarity. We report a case of bilateral traumatic knee dislocations with concomitant right hip dislocation and complete traumatic amputation of the left, nondominant upper extremity at the level of the proximal one-third of...

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Voos JE, Heyworth BE, Piasecki DP, et al. Traumatic bilateral knee dislocations, unilateral hip dislocation, and contralateral humeral amputation: a case report. HSS J. 2008;5(1):40-4doi: 10.1007/s11420-008-9100-9.
Voos, J. E., Heyworth, B. E., Piasecki, D. P., Henn, R. F., & MacGillivray, J. D. (2009). Traumatic bilateral knee dislocations, unilateral hip dislocation, and contralateral humeral amputation: a case report. HSS journal : the musculoskeletal journal of Hospital for Special Surgery, 5(1), 40-4. https://doi.org/10.1007/s11420-008-9100-9
Voos, James E, et al. "Traumatic bilateral knee dislocations, unilateral hip dislocation, and contralateral humeral amputation: a case report." HSS journal : the musculoskeletal journal of Hospital for Special Surgery vol. 5,1 (2009): 40-4. doi: https://doi.org/10.1007/s11420-008-9100-9
Voos JE, Heyworth BE, Piasecki DP, Henn RF, MacGillivray JD. Traumatic bilateral knee dislocations, unilateral hip dislocation, and contralateral humeral amputation: a case report. HSS J. 2009 Feb;5(1):40-4. doi: 10.1007/s11420-008-9100-9. Epub 2008 Dec 04. PMID: 19052715; PMCID: PMC2642548.
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Stereospecific and quantitative photodimerisation of terminal olefins in the solid state.

Chemical communications (Cambridge, England)

Georgiev IG, Bucar DK, Macgillivray LR.
PMID: 20517572
Chem Commun (Camb). 2010 Jul 21;46(27):4956-8. doi: 10.1039/c0cc01184c. Epub 2010 Jun 01.

Reaction of 4-vinylpyridine with AgClO(3) yields a crystalline solid that supports a stereospecific and quantitative [2+2] photodimerisation of two terminal olefins. Structural dynamics of the -CH[double bond, length as m-dash]CH(2) group, nature of the counterion, and extended packing influence...

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Georgiev IG, Bucar DK, Macgillivray LR. Stereospecific and quantitative photodimerisation of terminal olefins in the solid state. Chem Commun (Camb). 2010;46(27):4956-8doi: 10.1039/c0cc01184c.
Georgiev, I. G., Bucar, D. K., & Macgillivray, L. R. (2010). Stereospecific and quantitative photodimerisation of terminal olefins in the solid state. Chemical communications (Cambridge, England), 46(27), 4956-8. https://doi.org/10.1039/c0cc01184c
Georgiev, Ivan G, et al. "Stereospecific and quantitative photodimerisation of terminal olefins in the solid state." Chemical communications (Cambridge, England) vol. 46,27 (2010): 4956-8. doi: https://doi.org/10.1039/c0cc01184c
Georgiev IG, Bucar DK, Macgillivray LR. Stereospecific and quantitative photodimerisation of terminal olefins in the solid state. Chem Commun (Camb). 2010 Jul 21;46(27):4956-8. doi: 10.1039/c0cc01184c. Epub 2010 Jun 01. PMID: 20517572.
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FUNCTIONAL DIPLOPIA IN A SCHOOLBOY.

The British journal of ophthalmology

Macgillivray AM.
PMID: 18168765
Br J Ophthalmol. 1928 Nov;12(11):588-9. doi: 10.1136/bjo.12.11.588.

No abstract available.

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Macgillivray AM. FUNCTIONAL DIPLOPIA IN A SCHOOLBOY. Br J Ophthalmol. 1928;12(11):588-9doi: 10.1136/bjo.12.11.588.
Macgillivray, A. M. (1928). FUNCTIONAL DIPLOPIA IN A SCHOOLBOY. The British journal of ophthalmology, 12(11), 588-9. https://doi.org/10.1136/bjo.12.11.588
Macgillivray, A M. "FUNCTIONAL DIPLOPIA IN A SCHOOLBOY." The British journal of ophthalmology vol. 12,11 (1928): 588-9. doi: https://doi.org/10.1136/bjo.12.11.588
Macgillivray AM. FUNCTIONAL DIPLOPIA IN A SCHOOLBOY. Br J Ophthalmol. 1928 Nov;12(11):588-9. doi: 10.1136/bjo.12.11.588. PMID: 18168765; PMCID: PMC512067.
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The Necessity for an Exact Definition of Blindness (Classification of the Blind).

Proceedings of the Royal Society of Medicine

Macgillivray A.
PMID: 19978978
Proc R Soc Med. 1915;8:49-51.

No abstract available.

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Macgillivray A. The Necessity for an Exact Definition of Blindness (Classification of the Blind). Proc R Soc Med. 1915;8:49-51
Macgillivray, A. (1915). The Necessity for an Exact Definition of Blindness (Classification of the Blind). Proceedings of the Royal Society of Medicine, 849-51.
Macgillivray, A. "The Necessity for an Exact Definition of Blindness (Classification of the Blind)." Proceedings of the Royal Society of Medicine vol. 8 (1915): 49-51.
Macgillivray A. The Necessity for an Exact Definition of Blindness (Classification of the Blind). Proc R Soc Med. 1915;8:49-51. PMID: 19978978; PMCID: PMC2003592.
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THE ENTOMOLOGICAL SOCIETY OF AMERICA.

Science (New York, N.Y.)

Macgillivray AD.
PMID: 17835994
Science. 1915 Jun 04;41(1066):842-3. doi: 10.1126/science.41.1066.842.

No abstract available.

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Macgillivray AD. THE ENTOMOLOGICAL SOCIETY OF AMERICA. Science. 1915;41(1066):842-3doi: 10.1126/science.41.1066.842.
Macgillivray, A. D. (1915). THE ENTOMOLOGICAL SOCIETY OF AMERICA. Science (New York, N.Y.), 41(1066), 842-3. https://doi.org/10.1126/science.41.1066.842
Macgillivray, A D. "THE ENTOMOLOGICAL SOCIETY OF AMERICA." Science (New York, N.Y.) vol. 41,1066 (1915): 842-3. doi: https://doi.org/10.1126/science.41.1066.842
Macgillivray AD. THE ENTOMOLOGICAL SOCIETY OF AMERICA. Science. 1915 Jun 04;41(1066):842-3. doi: 10.1126/science.41.1066.842. PMID: 17835994.
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Showing 1 to 12 of 227 entries