Melbourne J. Schriver
About
Melbourne J. Schriver is a scholar working on Organic Chemistry, Inorganic Chemistry and Electronic, Optical and Magnetic Materials.
According to data from OpenAlex, Melbourne J. Schriver has authored 34 papers receiving a total of 551 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Organic Chemistry, 10 papers in Inorganic Chemistry and 9 papers in Electronic, Optical and Magnetic Materials. Recurrent topics in Melbourne J. Schriver's work include Synthesis and characterization of novel inorganic/organometallic compounds (7 papers), Inorganic and Organometallic Chemistry (6 papers) and Inorganic Fluorides and Related Compounds (5 papers). Melbourne J. Schriver is often cited by papers focused on Synthesis and characterization of novel inorganic/organometallic compounds (7 papers), Inorganic and Organometallic Chemistry (6 papers) and Inorganic Fluorides and Related Compounds (5 papers). Melbourne J. Schriver collaborates with scholars based in Canada, United Kingdom and United States. Melbourne J. Schriver's co-authors include Jack Passmore, Neil Burford, L. H. Sutcliffe, W. V. F. Brooks, Peter S. White, Simon Parsons, Xiaoping Sun, Simon A. Parsons, Hong‐Bin Du and Arthur J. Banister and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and Inorganic Chemistry.
In The Last Decade
Melbourne J. Schriver
32 papers receiving 452 citations
Peers
Melbourne J. Schriver
A. N. Chekhlov Russia
Hatsue Tamura Japan
D. Nalewajek United States
A. De Cian France
Théo Berclaz Switzerland
Mareike Gerenkamp Germany
Irina G. Irtegova Russia
Bert Lutz Netherlands
H. A. Kuska United States
Ian Lavender United Kingdom
Citations per year, relative to Melbourne J. Schriver Melbourne J. Schriver (= 1×)
peers
A. N. Chekhlov
Countries citing papers authored by Melbourne J. Schriver
Since
Specialization
Citations
This map shows the geographic impact of Melbourne J. Schriver's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Melbourne J. Schriver with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Melbourne J. Schriver more than expected).
Fields of papers citing papers by Melbourne J. Schriver
Since
Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences
This network shows the impact of papers produced by Melbourne J. Schriver. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Melbourne J. Schriver. The network helps show where Melbourne J. Schriver may publish in the future.
Co-authorship network of co-authors of Melbourne J. Schriver
This figure shows the co-authorship network connecting the top 25 collaborators of Melbourne J. Schriver. A scholar is included among the top collaborators of Melbourne J. Schriver based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Melbourne J. Schriver. Melbourne J. Schriver is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
1.
Masuda, Jason D., et al.. (2023). Synthesis and crystal structures of halogenated oxathiazolones and an unexpected propanamide. Acta Crystallographica Section C Structural Chemistry. 79(4). 125–132.
2.
Schriver, Melbourne J., et al.. (2017). Crystal structure determination as part of an ongoing undergraduate organic laboratory project: 5-[(E)-styryl]-1,3,4-oxathiazol-2-one. Acta Crystallographica Section E Crystallographic Communications. 73(9). 1298–1301.
3.
Schriver, Melbourne J., et al.. (2017). The crystal structures of two isomers of 5-(phenylisothiazolyl)-1,3,4-oxathiazol-2-one. Acta Crystallographica Section E Crystallographic Communications. 73(11). 1726–1731.
4.
Decken, A., Friedrich Grein, Aaron Mailman, et al.. (2016). Absorption of SO2(g) by TDAE[O2SSO2](s) to Give TDAE[O2SS(O)2SO2](s): Related Reactions of [NR4]2[O2SSO2](s) (R = CH3, C2H5). Inorganic Chemistry. 55(12). 5999–6009.
5.
Bruna, Pablo J., A. Decken, Friedrich Grein, et al.. (2013). Synthesis of (TDAE)(O2SSO2)(s) and Discovery of (TDAE)(O2SSSSO2)(s) Containing the First Polythionite, [O2SSSSO2]2–. Inorganic Chemistry. 52(23). 13651–13662.
6.
Du, Hong‐Bin, Robert C. Haddon, Ingo Krossing, et al.. (2002). Thermal hysteresis in dithiadiazolyl and dithiazolyl radicals induced by supercooling of paramagnetic liquids close to room temperature: a study of F3CCNSSN and an interpretation of the behaviour of F3CCSNSCCF3. Chemical Communications. 1836–1837.
7.
Brooks, W. V. F., Scott Brownridge, Jack Passmore, Melbourne J. Schriver, & Xiaoping Sun. (1996). Preparation and characterization of 1,3,2-dithiazolidine and 1,4-dithia-7-azabicyclo[2.2.1]heptane cations, and a mechanistic study of the cycloaddition reactions of alkenes with SNS. Journal of the Chemical Society Dalton Transactions. 1997–1997.
8.
Clyburne, Jason A. C. & Melbourne J. Schriver. (1996). 1,2-Addition Reaction of a Protic Phosphonium Cation with a Phosphaalkyne. Inorganic Chemistry. 35(10). 3062–3063.
9.
Bridson, John N., et al.. (1995). X-ray structure of 1,3-adamantane dicarbonamide. Journal of Chemical Crystallography. 25(1). 11–14.
10.
Burford, Neil, Jason A. C. Clyburne, Derek P. Gates, Melbourne J. Schriver, & John F. Richardson. (1994). Simple preparations of new monomeric trihalogenophosphine imides. Journal of the Chemical Society Dalton Transactions. 997–997.
11.
Brooks, W. V. F., T. Stanley Cameron, Simon Parsons, Jack Passmore, & Melbourne J. Schriver. (1994). Energetics of Formation and X-ray Crystal Structures of SNSNS(MF6)2 (M = As, Sb), Containing the Lattice-Stabilized, Aromatic, 6.pi. 1,3,4,2,5-Trithiadiazolium(2+) Cation Formed by the Crystal-Lattice-Enforced Symmetry-Allowed Cycloaddition of SN+ and SNS+. Inorganic Chemistry. 33(26). 6230–6241.
12.
Parsons, Simon A., Jack Passmore, Melbourne J. Schriver, & Xiaoping Sun. (1991). Quantitative preparations of 1,3,2-dithiazolium, 1,3,2,4-dithiadiazolium, and 1-halo-1,2,4,3,5-trithiadiazolium cations by the general, symmetry-allowed cycloadditions of SNSAsF6 with alkynes, nitriles, and thiazyl halides. Kinetics of cycloadditions of the 1,3-dipolar-like SNS+ with aliphatic and aromatic nitriles and alkynes. Inorganic Chemistry. 30(17). 3342–3348.
13.
Brooks, W. V. F., T. Stanley Cameron, Friedrich Grein, et al.. (1991). The energetics of formation and X-ray crystal structure of SNSNS(AsF6)2, containing the lattice-stabilized aromatic 6? 1,3,4,2,5-trithiadiazolium(2+) cation formed by the crystal-lattice-energy-driven, symmetry-allowed cycloaddition of SN+ and SNS+. Journal of the Chemical Society Chemical Communications. 1079–1079.
14.
Burford, Neil, et al.. (1991). Structure of bis[bis(trimethylsilyl)methylene]methoxyphosphorane. Acta Crystallographica Section C Crystal Structure Communications. 47(4). 884–886.
15.
Parsons, Simon, Jack Passmore, Melbourne J. Schriver, & Peter S. White. (1990). Cycloaddition reactions of dichlorodithionitronium hexafluoroarsenate(V) with alkynes and alkenes; the preparation and X-ray crystal structure of 1,3-dichloro-1,3,2-dithiazolidinium hexafluoroarsenate(V). Canadian Journal of Chemistry. 68(6). 852–862.
16.
Passmore, Jack & Melbourne J. Schriver. (1988). Investigation into the nature and chemistry of thiazyl chloride monomer and trimer (NSCL)n (n = 1,3) in solution using nitrogen-14 NMR spectroscopy, a useful routine tool for the characterization of small sulfur-nitrogen-containing compounds. Inorganic Chemistry. 27(16). 2749–2751.
17.
Burford, Neil, Jack Passmore, Melbourne J. Schriver, A. J. BANISTER, & L. H. Sutcliffe. (1987). The high yield synthesis of CF3CF3; A thermally stable, liquid radical, and the quantitative rearrangement of CF3 to CF3. Journal of Fluorine Chemistry. 35(1). 108–108.
18.
Apblett, Allen W., et al.. (1986). Convenient synthesis of thiazyl hexafluoroarsenate(V), [SN]+[AsF6]-, and small quantities of thiazyl fluoride, NSF. Inorganic Chemistry. 25(24). 4451–4452.
19.
Fairhurst, Shirley A., et al.. (1985). An ESR study of the polymerization of tetrahydrofuran with simple inorganic cations containing sulphur and nitrogen. Magnetic Resonance in Chemistry. 23(10). 828–831.
20.
Passmore, Jack, Ming Rao, Melbourne J. Schriver, et al.. (1985). Preparation of 1,3,2-dithiazolium hexafluoroarsenate(V), preparation and crystal structures of 5-methyl-1,3,2,4-dithiadiazolium and 4-methyl-1,3,2-dithiazolium hexafluoroarsenate(V) and the reduction of these salts to stable free radicals. Journal of the Chemical Society Dalton Transactions. 1405–1405.
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