Seeding innovation on nascent platforms: evidence from Amazon Alexa

Growing complementary innovations has always been a prominent concern for nascent platforms. With high uncertainty on the prosperity of the platform, complementors often hesitate to contribute innovation on the platform. This research studies complementor seeding strategy, which we define as “platform owners selectively fund third-party development of complementary innovation to elevate platform value”. We explore a mixed-methods design to examine Amazon Alexa’s seeding strategy from 2015 to 2021. Our preliminary findings reveal that complementor seeding could be conceptualized as a layered structure where the seeds are endorsed to grow innovation in platform applications, platform enablers, and platform foundation. Besides, a nascent platform will benefit from a shorter development window for seeding indirect complementary innovations that can give rise to undulating waves of innovation on the platform. Overall, this study contributes novel insights to digital innovation management on nascent platforms. </p

Supplementary document for Linearized EUV mask optimization based on adjoint method - 6872329.pdf

Supplement

Flowchart of study identification, inclusion, and exclusion.

<p>Flowchart of study identification, inclusion, and exclusion.</p

Summary ROC (SROC) curves for CTA and MRA.

<p>Summary ROC (SROC) curves for CTA and MRA.</p

Determination and Correlation of Dipyridamole p‑Toluene Sulfonate Solubility in Seven Alcohol Solvents and Three Binary Solvents

The solubility of dipyridamole p-toluene sulfonate in seven monosolvents (methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, isobutanol, 2-butanol) and three different binary solvents (methanol + ethanol, methanol + 1-propanol, methanol + 1-butanol) was measured by a gravimetric method at temperatures ranging from 288.15 to 328.15 K. The experimental results indicate that the solubility of dipyridamole p-toluene sulfonate increases with increasing temperature while showing negative correlation with the mole fraction of organic solvents (ethanol, 1-propanol, 1-butanol) at a given temperature in binary solvents. The Apelblat model, the CNIBS/R-K model, and the modified version of Jouyban-Acree models (the Apel-JA equation) were used to correlate the experimental data, and the calculated results of above models were found to agree well with the experimental data

Determination and Correlation of Dipyridamole p‑Toluene Sulfonate Solubility in Seven Alcohol Solvents and Three Binary Solvents

The solubility of dipyridamole p-toluene sulfonate in seven monosolvents (methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, isobutanol, 2-butanol) and three different binary solvents (methanol + ethanol, methanol + 1-propanol, methanol + 1-butanol) was measured by a gravimetric method at temperatures ranging from 288.15 to 328.15 K. The experimental results indicate that the solubility of dipyridamole p-toluene sulfonate increases with increasing temperature while showing negative correlation with the mole fraction of organic solvents (ethanol, 1-propanol, 1-butanol) at a given temperature in binary solvents. The Apelblat model, the CNIBS/R-K model, and the modified version of Jouyban-Acree models (the Apel-JA equation) were used to correlate the experimental data, and the calculated results of above models were found to agree well with the experimental data

Novel Strategy to Control Polymorph Nucleation of Gamma Pyrazinamide by Preferred Intermolecular Interactions during Heterogeneous Nucleation

Pyrazinamide is usually nucleated from solution as a dimeric form; it has rarely been reported in the γ form (chain structure) crystallized from solution, especially from aqueous solution. Here, we designed a novel way to obtain the γ form of pyrazinamide from aqueous solution. Specific templates were applied to disturb the intrinsic self-association of pyrazinamide molecules and prevent the formation of the dimer structure. In this paper, the heterosynthon design method was applied in pyrazinamide heterogeneous nucleation, in which sulfonamides were chosen as the templates. In the presence of sulfonamide templates, hydrogen bonds between the carbonyl moiety of the amide group in pyrazinamide molecules and the sulfonamide moiety of sulfonamide template molecules were formed; these preferred intermolecular interactions protected the carbonyl groups of PZA, facilitating assembly of PZA molecules in a chain via N–H···N′ and nucleating as the γ form of PZA. This is the first time that the heterosynthon design method was applied to screen effective templates, which can control and select the desired polymorph in heterogeneous nucleation

Supplementary document for Frequency properties of channeled spectropolarimetry: an information theory perspective - 6815704.pdf

Supplemental Documen

Polymorph Control by Investigating the Effects of Solvent and Supersaturation on Clopidogrel Hydrogen Sulfate in Reactive Crystallization

Reactive crystallization and polymorphic transformation of clopidogrel hydrogen sulfate (CHS) in nine pure solvents were studied at 313.15 K. It is found that thermodynamically stable polymorphic form tends to be obtained in solvents with higher solubility of CHS and the conversion rates from form I to form II are also mainly increased with increasing solubility. The solvent hydrogen bond donor ability is essential for determining the solvent effects on solubility and polymorphic formation of CHS. Besides, the reactive crystallization of CHS at different supersaturations in 2-propanol and 2-butanol was monitored online by using ATR-FTIR and FBRM with a calibration-based approach. The results indicate the nucleation induction period is the kinetic-determining stage and supersaturation is a direct factor to determine the polymorphic formation of CHS: form II was obtained with <i>s</i> under 18 while form I was produced when <i>s</i> increases above 21

Temperature-Sensitive Janus Particles PEG/SiO₂/PNIPAM-PEA: Applications in Foam Stabilization and Defoaming

The current study presents a scalable approach for the preparation of temperature-responsive PEG/SiO2/PNIPAM-PEA Janus particles and, for the first time, investigates their potential applications in stabilizing foam and defoaming by adjusting the temperature. The method utilizes a (W1 + O)/W2 emulsion system, which incorporates appropriate surfactants to stabilize the emulsion and prevent rapid dissolution of the hydrophilic triblock polymer PEG-b-PTEPM-b-PNIPAM in water. The PEG/SiO2/PNIPAM-PEA Janus particles with temperature-responsive characteristics were synthesized in a single step that combined the sol–gel reaction and photoinduced free radical polymerization. The contact angle of the hydrophilic PEG/SiO2/PNIPAM surface was measured to be 54.7 ± 0.1°, while the contact angle of the hydrophobic PEA surface was found to be 122.4 ± 0.1°. By incorporating PEG/SiO2/PNIPAM-PEA Janus particles at a temperature of 25 °C, the foam’s half-life is significantly prolonged from 42 s to nearly 30 min. However, with an increase in temperature to 50 °C, the foam’s half-life rapidly diminished to only 44 s. This innovative application effectively enhances foam stabilization at low temperatures and facilitates the rapid dissipation of foam at high temperatures